Hydrochloric Acid → (R)-1-(5-bromopyridin-3-yl)ethanol

온도

0 °C

A solution of (S)-(−)-α,α-diphenyl-2-pyrrolidinemethanol (253 mg, 1 mmol) and trimethyl borate (0.135 mL, 1.2 mmol) in tetrahydrofuran (10 mL) was stirred at room temperature for 1 hour after which time borane-methylsulfide complex (10 mL, 2M in tetrahydrofuran, 20 mmol) was added in one portion and the mixture cooled to 0° C. A solution of 3-acetyl-5-bromopyridine (2 g, 10 mmol) in tetrahydrofuran (10 mL) was added dropwise over 2 hours at 0° C. and then the mixture was allowed to warm to room temperature and was stirred overnight. After this time dilute aqueous hydrochloric acid (2M, 90 mL) was added with initial cooling and the mixture was stirred at room temperature for 2 hours. Dimethyl sulfide and tetrahydrofuran were removed under reduced pressure and the resulting yellow solution was basified to pH 11 with aqueous ammonia, extracted with ethyl acetate (3×50 mL) and the extracts washed with brine (50 mL), dried (MgSO4) and concentrated under reduced pressure to give (1R)-1-(5-bromopyridin-3-yl)ethanol (1.9 g) in acceptable purity.

1. additionwas added in one portion
2. temperatureto warm to room temperature
3. temperaturewith initial cooling
4. stirringthe mixture was stirred at room temperature for 2 hours
5. customDimethyl sulfide and tetrahydrofuran were removed under reduced pressure
6. extractionextracted with ethyl acetate (3×50 mL)
7. washthe extracts washed with brine (50 mL)
8. dry with materialdried (MgSO4)
9. concentrationconcentrated under reduced pressure

ORD 기록

ord-4cba110b59c5404ab60e6a841263e205

출처 데이터셋

uspto-grants-2013_06

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08461161B2