Org. Synth. 1946, 26, 50
DOI: 10.15227/orgsyn.026.0050
2-METHOXYDIPHENYL ETHER
[Benzene, 1-methoxy-2-phenoxy-]
Submitted by H. E. Ungnade and E. F. Orwoll.
Checked by Homer Adkins and E. E. Burgoyne.
1. Procedure
Powdered potassium hydroxide (29.4 g., 0.43 mole) is placed in a 500-ml. round-bottomed flask. Guaiacol (75 g., 0.60 mole) is added, and the mixture is allowed to react exothermically. After the reaction is complete, the mixture is stirred with a glass rod and then heated under reduced pressure for 3 hours at 150° in an oil bath (Note 1).
To the dry salt is added 0.3 g. of copper powder (Note 2), 81 g. (0.51 mole) of bromobenzene, and a few drops of guaiacol (Note 3). The mixture is stirred thoroughly with a glass rod; the flask is fitted with an air condenser and heated in a metal bath (Note 4). A reaction becomes evident at a bath temperature of 160–180°, liquefaction occurs, and the color of the mixture changes to red or purple. The temperature is gradually raised to 200° and maintained at 200° for 2 hours.
After cooling, the products are extracted from the reaction mixture with successive portions of water and ether. Extraction is facilitated by breaking up the solid material with a glass rod. The total amounts. of solvents required are approximately 750 ml. of water and 150 ml. of ether. The combined ether and water solutions are transferred to a 3-l. round-bottomed flask and steam-distilled with superheated steam maintained at 180–200°. After removal of the ether, 300 ml. of distillate is collected. This distillate contains the unreacted starting materials. Continued distillation gives 64–69 g. (62–67%) of crude solid 2-methoxydiphenyl ether in 14 l. of distillate. The product is filtered with suction and dried. Crystallization from a mixture of 600 ml. of low-boiling petroleum ether (b.p. 30–60°) and 435 ml. of higher-boiling petroleum ether (b.p. 60–70°) yields 54–61 g. of 2-methoxydiphenyl ether melting at 77–78°. Other 2-methoxydiphenyl ethers have been prepared by this procedure (Note 5).
2. Notes
1.
The salt of
guaiacol is heated under reduced pressure, in order to remove water, which is a negative catalyst in the Ullmann reaction.
1
2.
The
copper catalyst may be prepared by the method of Brewster and Groening.
2
3.
An excess of
guaiacol is essential. Weston and Adkins
1 have found that the
phenol,
copper, and air form the active catalyst in the Ullmann reaction.
4.
The checkers used an electrically heated oil bath.
5.
Yields of
54% of
2-methoxy-4'-methyldiphenyl ether from
p-bromotoluene and
guaiacol, and
60% of
2-methoxy-5-methyldiphenyl ether from
3-bromo-4-methoxytoluene and
phenol, have been obtained by the same method in the laboratory of the submitters.
3. Discussion
The procedure above is a modification of the method of Ullmann and Stein
3 for the same compound. Sartoretto and Sowa
4 used the same general method. The need for a catalyst can be avoided by heating a mixture of
guaiacol potassium, guaiacol, and chlorobenzene at 200° under pressure.
5 Ullmann and Stein
6 have prepared the compound by using
phenol,
o-bromoanisole,
copper powder, and
potassium hydroxide.
2-Hydroxydiphenyl ether can be converted to the methoxy derivative by treating it with
methanol,
methyl iodide, and
potassium hydroxide.
7
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
petroleum ether
methanol (67-56-1)
ether (60-29-7)
phenol (108-95-2)
copper,
copper powder (7440-50-8)
chlorobenzene (108-90-7)
potassium hydroxide (1310-58-3)
bromobenzene (108-86-1)
Guaiacol (90-05-1)
Methyl iodide (74-88-4)
2-Methoxydiphenyl ether,
Benzene, 1-methoxy-2-phenoxy- (1695-04-1)
2-methoxy-5-methyldiphenyl ether
3-bromo-4-methoxytoluene (22002-45-5)
guaiacol potassium
2-Hydroxydiphenyl ether
p-Bromotoluene (106-38-7)
o-bromoanisole (578-57-4)
2-methoxy-4'-methyldiphenyl ether
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