Hydrochloric Acid → 4-(Methoxymethoxy)phenol

Temperature

-20 °C

A mixture of 60% sodium hydride (1.80 g, 45.0 mmol) and dry THF (20 mL) was cooled to −20° C. After addition of a solution of hydroquinone (2.00 g, 18.2 mmol) in THF (30 mL), the mixture was stirred at room temperature for one hour and then cooled again to −20° C. After dropwise addition of chloromethyl methyl ether (1.3 mL, 18.0 mmol), the cooled mixture was slowly warmed to 10° C., stirred at room temperature for one hour, and poured onto ice pieces (500 g). To the resulting mixture was added 3 mol/L aqueous hydrochloric acid until the mixture reached pH 4-5. Subsequently, the mixture was subjected to extraction with dichloromethane (100 mL×2). The extract was washed with water (100 mL×2) and saturated aqueous sodium chloride (100 mL), dried over anhydrous sodium sulfate, and placed under reduced pressure to distill the solvent off. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), to obtain 581 mg (yield 21%) of the titled compound as pale yellow oil.

1. temperaturecooled again to −20° C
2. temperaturethe cooled mixture was slowly warmed to 10° C.
3. stirringstirred at room temperature for one hour
4. additionpoured onto ice pieces (500 g)
5. extractionSubsequently, the mixture was subjected to extraction with dichloromethane (100 mL×2)
6. washThe extract was washed with water (100 mL×2) and saturated aqueous sodium chloride (100 mL)
7. dry with materialdried over anhydrous sodium sulfate
8. distillationto distill the solvent off
9. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

ORD record

ord-211ef401f8134456bfc4140a1d5e4d52

Source dataset

uspto-grants-2009_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07598254B2