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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854144Generated: November 1, 2026

4-Aminopyridine → HCID 86605369, compound

https://huagongshe.com/reaction/854144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantEthyl AcetateHCID 8857—
Reactant(2S)-2-butyloxiraneHCID 1549991—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178418416HCID 178418416—
SolventEthanolHCID 702—
ProductHCID 86605369HCID 8660536985%

Reaction Steps

In a 50 mL-volumetric autoclave were added deaerated ethanol (10 mL) and ethyl acetate (10 mL), and thereto were added 4-aminopyridine (47 mg, 0.5 mmol) and (S)-1,2-epoxyhexane (2.0 g, 20 mmol, >99% ee). Then to the mixture was added crystalline dicobaltoctacarbonyl complex (171 mg, 0.5 mmol). After covering the autoclave with a cap, carbon monoxide (1 MPa) and hydrogen gas (1 MPa) were introduced therein and the mixture was reacted at 35° C. for 28 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-3-hydroxyheptanoic acid ethyl ester (2.92 g, 85%, >99% ee) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256305B2
Source datasetuspto-grants-2007_08
ORD IDord-ae50dea6e51241bc8778130daca9d8e9
Source noteuspto-grants-2007_08