Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785279Generated: November 1, 2026

Acetic Anhydride → HCID 69076131, compound

https://huagongshe.com/reaction/1785279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantHCID 69075646HCID 69075646—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 69076131HCID 69076131—

Reaction Steps

To a solution of 42 mg of t-butyl 4-((2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-(hydroxymethyl)phenyl)-ethanoyloxy)tetrahydropyridine-1(2H)-carboxylate in 2 ml of chloroform, 0.015 ml of triethylamine, 0.01 ml of acetic anhydride and 2 mg of dimethylaminopyridine were added successively, followed by an hour's stirring at room temperature. The reaction liquid was diluted with ethyl acetate, washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resulting residue was purified on preparative thin layer chromatography (Kieselgel™ 60F254, Art 5744 (Merck), hexane/ethyl acetate=2/1) to provide 42 mg of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504432B2
Source datasetuspto-grants-2009_03
ORD IDord-de7e1269efe741ef877a9100d62df71e
Source noteuspto-grants-2009_03