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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228Generated: October 26, 2026

Water → N-(1-Benzylpiperidin-4-yl)acetamide

https://huagongshe.com/reaction/2228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
SolventDichloromethaneHCID 6344—
ProductN-(1-Benzylpiperidin-4-yl)acetamideHCID 12641850—

Reaction Steps

Acetyl chloride (3.95 ml) was added dropwise to a stirred solution of 4-amino1-benzylpiperidine (10.0 g) and triethylamine (7.7 ml) in dry dichloromethane (100 ml) at 4° C. The mixture was allowed to reach ambient temperature and stirred for 16 hours. Water was then added, the organic phase separated and dried (MgSO4), and removal of the solvent by evaporation gave 4-acetylamino-1-benzylpiperidine, 10.23 g, as a light brown solid which was used without further purification: NMR (CDCl3) δ 7.29(5H,m), 5.29(1H,b), 3.79(1H,m), 3.49(2H,s), 2.80(2H,dm), 2.12(2H,dt), 1.95(3H,s), 191(2H,dm), 1.46(2H,dq); m/e 233 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728701
Source datasetuspto-grants-1998_03
ORD IDord-53468aff36b74b69af45a0218b9d4c73
Source noteuspto-grants-1998_03