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Org. Synth. 1997, 74, 108
DOI: 10.15227/orgsyn.074.0108
DIETHYL (DICHLOROMETHYL)PHOSPHONATE. PREPARATION AND USE IN THE SYNTHESIS OF ALKYNES: (4-METHOXYPHENYL)ETHYNE
[Phosphonic acid, (dichloromethyl)-, diethyl ester to prepare Benzene, 1-ethylnyl-4-methoxy-]
Submitted by Angela Marinetti and Philippe Savignac1.
Checked by Catherine Dubuisson and Louis S. Hegedus.
1. Procedure
A. Diethyl (dichloromethyl)phosphonate, 1. An oven-dried, 1-L, four-necked, round-bottomed flask (or a 1-L, three-necked flask with a Claisen head fitted in a side neck) is fitted with an efficient mechanical stirrer, thermometer, reflux condenser with a bubbler, and a 200-mL, pressure-equalizing addition funnel with a nitrogen inlet. Under a gentle flow of nitrogen the flask is charged with 400 mL of tetrahydrofuran (THF) (Note 1). The addition funnel is charged with a 1.9 M solution of isopropylmagnesium chloride in diethyl ether (83 mL, 0.158 mol) (Note 2). The mixture is cooled to −78°C with a dry ice/acetone bath (Note 3), and isopropylmagnesium chloride is added over a few minutes with stirring. At this temperature, a solution of diethyl (trichloromethyl)phosphonate (38.3 g, 0.150 mol) (Note 4) in tetrahydrofuran (50 mL) is added dropwise over 15 min. The resulting solution is stirred for an additional 15 min at −78°C producing a clear orange solution. Anhydrous ethanol (12 g, 0.260 mol) in tetrahydrofuran (15 mL) is added dropwise at −78°C, producing a clear yellow solution. The resulting mixture is stirred for a few minutes, then allowed to warm slowly to −40°C. The reaction mixture is poured into a beaker containing a stirred mixture of 3 M hydrochloric acid (70 mL), and an equal volume of crushed ice and dichloromethane (70 mL). The yellow color initially dissipates, but the solution becomes yellow orange upon warming to room temperature. The organic layer is separated, and the aqueous layer is extracted with dichloromethane (2 × 60 mL). The extracts are combined and dried over anhydrous magnesium sulfate. After the filtration, the solvents are evaporated on a rotary evaporator. The bright yellow, crude liquid (36.3 g) is transferred to a pear-shaped flask fitted with a 10-cm Vigreux column and distilled under reduced pressure to give 26.6 g (80%) of diethyl (dichloromethyl)phosphonate, 1, as a pale yellow liquid, bp 115–119°C/9 mm, >90% pure by 1H, 13C and 31P NMR spectroscopy (Note 5) and (Note 6).
B. (4-Methoxyphenyl)ethyne, 2. An oven-dried, 1-L, four-necked, round-bottomed flask is fitted as above, flushed with nitrogen, and charged with a solution of butyllithium in hexane (1.56 M, 92 mL, 0.143 mol) (Note 7). The solution is cooled with stirring to −20°C with a dry ice/acetone bath and a solution of diisopropylamine (15.1 g, 0.149 mol) (Note 8) in tetrahydrofuran (220 mL) (Note 1), is added dropwise over 15 min. The resulting clear solution is cooled to −78°C and treated by the dropwise addition of a solution of 1 (30 g, 0.136 mol) and 4-methoxybenzaldehyde (18.1 g, 0.133 mol) (Note 8) in tetrahydrofuran (60 mL) over 30 min. The resulting brown solution is stirred at −78°C for an additional 30 min, then allowed to warm slowly to 0°C over 60 min. The resulting mixture is then cooled to −78°C and a solution of butyllithium (1.56 M in hexane, 183 mL, 0.285 mol) (Note 7) is added dropwise over 20 min. The resulting brown solution is stirred at −78°C for an additional 30 min, then allowed to warm slowly to 0°C over 60 min. At this temperature, the reaction mixture is quenched by the dropwise addition of 3 M hydrochloric acid to pH 5–6 (125–130 mL). The brown color has practically disappeared and the solution is yellow orange. The organic layer is separated and the aqueous layer is extracted with diethyl ether (3 × 50-mL). The extracts are combined, washed with water (3 × 10 mL), and dried over anhydrous magnesium sulfate. Magnesium sulfate is removed by filtration and the solvents are evaporated on a rotary evaporator. The residue is dissolved in hexane (200 mL) and filtered after 30 min. Solvent is again completely evaporated under reduced pressure. Crude product 2 thus obtained is purified by column chromatography on silica gel (Note 9) to afford 11.0 g (63%) of pure (4-methoxyphenyl)ethyne as a colorless liquid, bp 70–72°C (3 mm) that gives white crystals on standing in the freezer (Note 10).
2. Notes
1. Tetrahydrofuran is obtained from S.D.S. Company and is purified by distillation from sodium and benzophenone.
2. Isopropylmagnesium chloride (2 M in diethyl ether) is available from Aldrich Chemical Company, Inc., and is standardized before use by titration against a solution of benzyl alcohol in toluene with cuproine (2,2'-biquinoline).
3. An alternative cooler was also used by the submitters consisting of a Dewar partially filled with liquid nitrogen.
4. Diethyl (trichloromethyl)phosphonate (97%) either purchased from Aldrich Chemical Company, Inc., or prepared according to a described procedure2 is used.
5. The crude liquid could be distilled using a Kugelrohr apparatus. The main fraction (27.5 g, 83% yield) consists of a clear orange liquid that was collected at 145–155°C (oven temperature)/9–10 mm. 1H NMR (200 MHz, CDCl3) indicates that this material is of the same purity as that from conventional distillation.
6. The product displays the following spectroscopic data: 31P NMR (81 MHz, CDCl3) δ: +10.9; 1H NMR (200 MHz, CDCl3) δ: 1.29 (t, 6 H, CH3), 4.22 (dq, 4 H, CH2), 5.6 (d, 1 H, 2JH-P = 2, CH); 13C NMR (50 MHz, CDCl3) δ: 16.2 (d, JC-P = 5.9, CH3), 60.7 (d, JC-P = 178, CH), 65.0 (d, JC-P = 7.4, CH2) ppm.
7. Butyllithium (1.6 M solution in hexane) is available from Janssen Chimica or Aldrich Chemical Company, Inc., and is standardized before use by titration against a solution of benzyl alcohol in toluene with cuproine (2,2'-biquinoline) or with (±)-2-butanol and 1,10-phenanthroline in diethyl ether.
8. Diisopropylamine (99%) and 4-methoxybenzaldehyde (98%) were purchased from Aldrich Chemical Company, Inc., and used without purification.
9. The crude product is purified by chromatography (200 g of silica gel, Silitech 32–63 μm, purchased from ICN Biomedicals; column diameter, 5.5 cm). Elution is performed first with hexanes (200 mL) and then with hexanes-diethyl ether (20:1). Alternatively, the submitters purified the product by distillation from a pear-shaped flask using an 8-cm fractionating column.
10. The product displays the following spectroscopic data: 1H NMR (200 MHz, CDCl3) δ: 3.02 (s, 1 H), 3.80 (s, 3 H), 6.8 (AA'BB', 2 H), 7.4 (AA'BB', 2 H); 13C NMR (50, MHz, CDCl3) δ: 55.2 (OCH3), 75.8 (CCH), 83.6 (CCH), 113.9 [CH (Ar)], 114.0 (C-C≡CH), 133 [CH (Ar)], 159.9 (COCH-3) ppm.
Handling and Disposal of Hazardous Chemicals
The procedures in this article are intended for use only by persons with prior training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011 www.nap.edu). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices.
These procedures must be conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein.
3. Discussion
The procedure described in Part A represents a convenient synthesis ofdiethyl (dichloromethyl)phosphonate, 1, for large-scale preparations (up to 1 mol). The use of isopropylmagnesium chloride instead of butyllithium3,4 reduces the amount of by-products,5 simplifies the purification step, and improves the yield. An alternative synthetic method for 1 is chlorination of diethyl (chloromethyl)phosphonate;6,7 however, yields and selectivities are lower than in the procedure described here. Diethyl (dichloromethyl)phosphonate, 1, or the corresponding lithiated derivative, are useful intermediates in organic synthesis: 1,1-dichloroalkenes3,4,6 as well as terminal alkynes4 have been prepared.
Part B shows the use of 1 as starting material for the synthesis of (4-methoxyphenyl)ethyne. The generation of the phosphorylated carbanion is performed through metalation with lithium diisopropylamide (LDA). A mixture containing the phosphorus reagent 1 and the aldehyde is added directly to LDA, in order to trap the unstable phosphorylated, lithiated carbanion, thus preventing decomposition and side reactions. The formation of (4-methoxyphenyl)ethyne described here is an example of a general synthetic method for the conversion of aldehydes into acetylenes, on a large scale, by means of diethyl (dichloromethyl)phosphonate, 1. The methodology is well suited for the synthesis of a wide variety of acetylenic compounds, such as C9H19C≡CH, (C2H5)2CHC≡CH, C6H5CH=CHC≡CH,4 and analogous terminal alkynes. Several methods for the preparation of alkynes based on phosphorus reagents have been reported previously. Each of these procedures can be regarded as an extension of the Wittig-Horner olefin synthesis. In the final step the olefins are converted into the corresponding alkynes. The first method that employed the PPh3-CBr4 couple (or PPh3- CBr4- zinc dust) was introduced by Corey and Fuchs8 (1972). The amounts of PPh3 involved (2 or 4 equiv and of PPh3O formed during the reaction, are obstacles for large scale synthesis. Dimethyl diazomethylphosphonate first prepared by Seyferth9 in 1971 was shown, by Colvin and Hamill10 in 1977, then by Gilbert and Weerasooriya11 in 1982, to be an effective reagent for the transformation of aldehydes, alkyl aryl ketones or diaryl ketones into alkynes. However, this reagent is rather difficult to prepare (four steps, 46% yield), and very hazardous to handle (explosive decomposition on distillation), and therefore is unsuitable for preparative scale synthesis.

References and Notes
  1. Hétéroséléments et Coordination, URA CNRS 1499, DCPH, Ecole Polytechnique, 91128 Palaiseau Cedex, France.
  2. Kosolapoff, G. M. J. Am. Chem. Soc. 1947, 69, 1002
  3. Seyferth, D.; Marmor R. S. J. Organometal. Chem. 1973, 59, 237
  4. Villieras, J.; Perriot, P.; Normant J. F. Synthesis 1975, 458
  5. Lowen, G. T.; Almond, M. R. J. Org. Chem. 1994, 59, 4548.
  6. Savignac, Ph.; Dreux, M.; Coutrot, Ph. Tetrahedron Lett. 1975, 609
  7. Lee, K.; Shin, W.S.; Oh, D. Y. Synth. Comm. 1991, 21, 1657
  8. Corey, E. J.; Fuchs, P. L. Tetrahedron Lett. 1972, 3769
  9. Seyferth, D.; Marmor, R. S.; Hilbert, P. J. Org. Chem. 1971, 36, 1379.
  10. Colvin, E. W.; Hamill, B. J. J. Chem. Soc., Perkin Trans. 1 1977, 869.
  11. Gilbert, J. C.; Weerasooriya, U. J. Org. Chem. 1982, 47, 1837.

Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)

Benzene, 1-ethylnyl-4-methoxy-

sodium and benzophenone

cuproine

ethanol (64-17-5)

hydrochloric acid (7647-01-0)

diethyl ether (60-29-7)

nitrogen (7727-37-9)

toluene (108-88-3)

zinc (7440-66-6)

Benzyl alcohol (100-51-6)

dichloromethane (75-09-2)

magnesium sulfate (7487-88-9)

isopropylmagnesium chloride (1068-55-9)

butyllithium (109-72-8)

Tetrahydrofuran (109-99-9)

hexane (110-54-3)

(±)-2-butanol (78-92-2)

lithium diisopropylamide (4111-54-0)

1,10-phenanthroline (66-71-7)

diisopropylamine (108-18-9)

4-methoxybenzaldehyde (123-11-5)

2,2'-biquinoline (119-91-5)

Dimethyl diazomethylphosphonate

Diethyl (dichloromethyl)phosphonate,
Phosphonic acid, (dichloromethyl)-, diethyl ester (3167-62-2)

(4-Methoxyphenyl)ethyne (768-60-5)

diethyl (trichloromethyl)phosphonate (866-23-9)

diethyl (chloromethyl)phosphonate (3167-63-3)