Pyridine → Carbonic acid 1-chloroethyl ester (1R,2R)-2-methylcyclohexyl ester

To a mixture of 1-chloroethyl chloroformate [CSA No. 50893-53-3] (0.416 mL), pyridine (0.624 mL), and THF (25 mL), (1R,2R)-2-methylcyclohexanol [CSA No. 19043-03-9] (441 mg) dissolved in THF (5 mL) was added at −78° C. After stirring the mixture overnight at room temperature, ethyl acetate (100 mL) and heptane (100 mL) were added to the mixture. The resulting mixture was sequentially washed with 0.5 N hydrochloric acid (50 mL), saturated aqueous sodium hydrogen carbonate solution (50 mL), water (50 mL), and saturated aqueous sodium chloride solution (50 mL), and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure to obtain the captioned compound (482 mg).

1. additionwas added at −78° C
2. washThe resulting mixture was sequentially washed with 0.5 N hydrochloric acid (50 mL), saturated aqueous sodium hydrogen carbonate solution (50 mL), water (50 mL), and saturated aqueous sodium chloride solution (50 mL)
3. dry with materialdried over anhydrous magnesium sulfate
4. filtrationThe resulting mixture was filtered
5. customthe filtrate obtained
6. concentrationwas concentrated under reduced pressure

ORD-Eintrag

ord-87eccb2d1671482eaca09ac69578aa9c

Quelldatensatz

uspto-grants-2013_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08436009B2