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HRID 911435作成日:2026年10月27日

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

https://huagongshe.com/reaction/911435

反応式

関与物質

役割名称HCID仕込み量
反応物Vinyl AcetateHCID 7904—
反応物Potassium CarbonateHCID 11430—
反応物1-(6-Methylpyridin-2-yl)ethanolHCID 353138—
反応物(R)-acetic acid 1-(6-methyl-pyridin-2-yl)-ethyl esterHCID 131729192—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Diisopropyl EtherHCID 7914—
溶媒Sodium chloride; waterHCID 57417360—
生成物(R)-1-(6-methylpyridin-2-yl)ethanolHCID 4507948489%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022062B2
出典データセットuspto-grants-2011_09
ORD IDord-30abc6d928cc4f8d8743af3433dfe1cd
出典メモuspto-grants-2011_09