Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829177Generated: November 2, 2026

Acetic Anhydride → HCID 22061397, compound

https://huagongshe.com/reaction/1829177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 3-(aminomethyl)azetidine-1-carboxylateHCID 10679125—
SolventDichloromethaneHCID 6344—
ProductHCID 22061397HCID 22061397—

Reaction Steps

Triethylamine (0.76 ml, 5.45 mmol) and acetic anhydride (0.43 ml, 4.56 mmol) were added to an ice-cooled solution of tert-butyl 3-(aminomethyl)-1-azetidinecarboxylate (J. Med. Chem. 2001; 44(1); 94) (850 mg, 4.56 mmol) in dichloromethane (50 ml), and the reaction stirred for 30 minutes. The solution was washed with water (50 ml), brine (50 ml), dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using ethyl acetate as eluant to afford the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060836B2
Source datasetuspto-grants-2006_06
ORD IDord-36e25a305e5142b2b161e92562b5576e
Source noteuspto-grants-2006_06