Hydrochloric Acid → 2-(1-Ethylcyclohexyl)ethanol

After adding a 1.0 M tetrabutylammonium fluoride-tetrahydrofuran solution (7.70 mL, 7.70 mmol) to a solution of tert-butyl-2-(1-ethylcyclohexyl)ethoxydiphenylsilane (3.02 g, 7.65 mmol) in tetrahydrofuran (20 mL) at room temperature, the mixture was stirred for 2 hours. A 1.0 M tetrabutylammonium fluoride tetrahydrofuran solution (7.70 mL, 7.70 mmol) was then added, and the mixture was stirred for 14 hours. After further adding 1N hydrochloric acid (20 mL) to the reaction mixture, extraction was performed with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the organic layer was dried over anhydrous magnesium sulfate. After filtering and concentration under reduced pressure, the obtained residue was purified by silica gel column chromatography (100 g Merck Art. 9385, hexane:ethyl acetate=6:1) to obtain the title compound as a colorless oil (708 mg) (3 steps, 57% yield).

1. stirringthe mixture was stirred for 14 hours
2. extractionto the reaction mixture, extraction
3. washThe organic layer was washed with saturated aqueous sodium chloride
4. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
5. filtrationAfter filtering
6. concentrationconcentration under reduced pressure
7. customthe obtained residue was purified by silica gel column chromatography (100 g Merck Art. 9385, hexane:ethyl acetate=6:1)

ORD record

ord-96417a859b5f47088989dc27b0ec0ce9

Source dataset

uspto-grants-2009_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07601843B2