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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 911435생성일: 2026년 10월 26일

Vinyl Acetate → (R)-1-(6-methylpyridin-2-yl)ethanol

https://huagongshe.com/reaction/911435

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl AcetateHCID 7904—
반응물Potassium CarbonateHCID 11430—
반응물1-(6-Methylpyridin-2-yl)ethanolHCID 353138—
반응물(R)-acetic acid 1-(6-methyl-pyridin-2-yl)-ethyl esterHCID 131729192—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Diisopropyl EtherHCID 7914—
용매Sodium chloride; waterHCID 57417360—
생성물(R)-1-(6-methylpyridin-2-yl)ethanolHCID 4507948489%

반응 단계

Stir a mixture of 1-(6-methyl-pyridin-2-yl)-ethanol (2.9 g, 21 mmol), 4 A molecular sieves powder (3 g), vinyl acetate (6 mL) and lipase Candida Antarctica acrylic resin (0.87 g) in i-Pr2O (40 mL) at ambient temperature overnight (J. Org. Chem. 1998, 63, 2481-2487; Synlett 1999, 41-44). Remove the solid residue by filtration. Evaporate the volatile substances and purify by chromatography eluting with hexane/EtOAc (7:3 to 1:1) to give the faster eluting (R)-acetic acid 1-(6-methyl-pyridin-2-yl)-ethyl ester as colorless oil (1.9 g, 50%), and the slower eluting (S)-alcohol as light yellow oil (1.258 g, 43%). Dissolve (R)-acetic acid 1-(6-methyl-pyridin-2-yl)-ethyl ester (1.72 g, 9.62 mmol) in methanol (50 mL) and add potassium carbonate (5.3 g, 38.5 mmol) in water (10 mL). Stir the mixture at ambient temperature for 4 h. Dilute with brine, extract three times with EtOAc, dry over anhydrous Na2SO4, filter through a short pad of silica gel and concentrate in vacuo to give the desired intermediate as a colorless oil (1.17 g, 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08022062B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-30abc6d928cc4f8d8743af3433dfe1cd
출처 메모uspto-grants-2011_09