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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854149Generated: October 31, 2026

4-Aminopyridine → HCID 11052254, compound

https://huagongshe.com/reaction/854149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantTetrahydrofuranHCID 8028—
Reactant(+)-EpichlorohydrinHCID 149428—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178418416HCID 178418416—
CatalystRhodiumHCID 23948—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
SolventIsopropanolHCID 3776—
ProductHCID 11052254HCID 1105225492%

Reaction Steps

In a 50 mL-volumetric autoclave were added deaerated isopropanol (10 mL) and THF (10 mL), and thereto were added cobalt acetate tetrahydrate (250 mg, 1 mmol) and 10% Rh/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 100° 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 (1.3 MPa) was introduced therein and the mixture was reacted at 35° C. for 30 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-4-chloro-3-hydroxybutanoic acid isopropyl ester (3.3 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-28fc7587e4a54ef09833bd79cb9189c0
Source noteuspto-grants-2007_08