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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232088Generated: October 31, 2026

Acetyl chloride → 3-Acetylaminomethyl-1-benzyl-4-chloropyrrolidine

https://huagongshe.com/reaction/2232088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Aminomethyl-1-benzyl-4-chloropyrrolidineHCID 13959895—
SolventEthanolHCID 702—
Product3-Acetylaminomethyl-1-benzyl-4-chloropyrrolidineHCID 1391300878.3%

Reaction Steps

To 3-aminomethyl-1-benzyl-4-chloropyrrolidine (2.69 g) is added ethanol (50 ml) and thereto is added dropwise acetyl chloride (1.02 g) with stirring under ice-cooling. The mixture is stirred at room temperature overnight, then concentrated, neutralized with saturated aqueous sodium hydrogen carbonate, and extructed with dichloromethane. The dichloromethane layer is dried and concentrated to give 3-acetylaminomethyl-1-benzyl-4-chloropyrrolidine (2.50 g) as an yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04786649
Source datasetuspto-grants-1988_11
ORD IDord-ada00a0e55684e659624752873a26ccc
Source noteuspto-grants-1988_11