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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854148Generated: October 31, 2026

Ethanol → Ethyl (3S)-4-chloro-3-hydroxybutanoate

https://huagongshe.com/reaction/854148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-AminopyridineHCID 1727—
Reactant(+)-EpichlorohydrinHCID 149428—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178418416HCID 178418416—
CatalystPalladiumHCID 23938—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
ProductEthyl (3S)-4-chloro-3-hydroxybutanoateHCID 701927792%

Reaction Steps

In a 50 mL-volumetric autoclave were added deaerated ethanol (10 mL), and thereto were added cobalt acetate tetrahydrate (250 mg, 1 mmol) and 10% Pd/C (10 mg). After covering the autoclave with a cap, carbon monoxide (1 MPa) and hydrogen gas (1 MPa) were introduced therein, successively and the mixture was reacted at 80° C. for 3 hours. After 3 hours the mixture was cooled to room temperature, and the mixed gas was emitted to give a solution containing dicobaltoctacarbonyl complex. Thereto were added 4-aminopyridine (47 mg, 0.5 mmol) and (S)-epichlorohydrin (1.8 g, 20 mmol, >99% ee). After covering the autoclave with a cap, carbon monoxide (1 MPa) was introduced therein and the mixture was reacted at 35° C. for 28 hours. After temperature of the mixture was made room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-4-chloro-3- hydroxybutanoic acid ethyl ester (3.1 g, 92%, >99% ee) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256305B2
Source datasetuspto-grants-2007_08
ORD IDord-ce03cb5de30f4da7a7517cfa7311d7ef
Source noteuspto-grants-2007_08