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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626129Generated: October 30, 2026

Acetic Anhydride → 3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl Acetate

https://huagongshe.com/reaction/1626129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Chloro-6,7-dihydro-5h-cyclopenta[b]pyridine 1-oxideHCID 58082839—
Product3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl AcetateHCID 58082768—

Reaction Steps

A solution of 3-chloro-6,7-dihydro-5H-[1]pyrindine 1-oxide (2.07 g, 12.2 mmol) in acetic acid anhydride (62.2 ml, 659 mmol) was stirred at 110° C. for 20 hours. For the workup, the solvent was removed at reduced pressure and the residue quenched with saturated aqueous solution of sodium hydrogen carbonate. The aqueous phase was extracted with dichloromethane, the resulting organic layers combined and dried over sodium sulphate. After evaporation of the solvent, the residue was purified by flash chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 70:30 as the eluent. The acetic acid 3-chloro-6,7-dihydro-5H-[1]pyrindin-7-yl ester was obtained as a red liquid (1.57 g, 61% yield). MS (ISP): m/z=212 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785436B2
Source datasetuspto-grants-2014_07
ORD IDord-29dcf8eb214f42309180d128712792da
Source noteuspto-grants-2014_07