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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911441Generated: October 29, 2026

Vinyl Acetate → (1R)-1-(Pyridin-2-yl)ethan-1-ol

https://huagongshe.com/reaction/911441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
ReactantPotassium CarbonateHCID 11430—
Reactantalpha-Methyl-2-pyridinemethanolHCID 86784—
ReactantHCID 13138793HCID 13138793—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiisopropyl EtherHCID 7914—
SolventSodium chloride; waterHCID 57417360—
Product(1R)-1-(Pyridin-2-yl)ethan-1-olHCID 64284789%

Reaction Steps

Stir a mixture of (±)-1-(pyridin-2-yl)-ethanol (21.2 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-(pyridin-2-yl)-ethyl ester as colorless oil (50%) and the slower eluting (S)-alcohol as light yellow oil (43%). Dissolve (R)-acetic acid 1-(pyridin-2-yl)-ethyl ester (9.620 mmol) in methanol (50 mL) and add potassium carbonate (38.48 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 (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-25c25f32dc544346857b1ad1b5562bf3
Source noteuspto-grants-2011_09