Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778410Generated: November 1, 2026

Acetic Anhydride → Tert-butyl 3-acetoxyazetidine-1-carboxylate

https://huagongshe.com/reaction/1778410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-acetoxyazetidine-1-carboxylateHCID 5833403994.2%

Reaction Steps

A solution of tert-butyl 3-hydroxyazetidine-1-carboxylate (2.0 g), DMAP (1.55 g) and triethylamine (2.34 g) in DCM (80 mL) was cooled to 0° C. A solution of acetic anhydride (2.35 g) in DCM (20 mL) was added dropwise over 20 minutes and the reaction mixture was stirred at room temperature for 1 hour. The mixture was washed with water and brine, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was dissolved in ether and washed with 10% aqueous citric acid solution and brine, dried (MgSO4), filtered. The filtrate was concentrated in vacuo to give tert-butyl 3-acetoxyazetidine-1-carboxylate (2.34 g) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-fe89f9c90bf44376b177bb1378f86739
Source noteuspto-grants-2016_02