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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409885Generated: October 29, 2026

Benzoyl chloride → HCID 66601302, compound

https://huagongshe.com/reaction/409885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 3-aminoazetidine-1-carboxylateHCID 1516507—
SolventDichloromethaneHCID 6344—
ProductHCID 66601302HCID 6660130298.5%

Reaction Steps

To a solution of 1-Boc-3-aminoazetidine 1a (1.2 g, 6.98 mmol) and Et3N (2.4 mL, 17.3 mmol) in CH2Cl2 (70 mL) at 0° C. was added benzoyl chloride 1b (0.89 mL, 7.68 mmol). The reaction was kept at 0° C. for 3 h, quenched with aq. NaHCO3, and the resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by flash column chromatography (silica gel, 40% EtOAc/heptane) gave compound 1c (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759533B2
Source datasetuspto-grants-2014_06
ORD IDord-536a936dba024c3ea51e58cd1bef98f8
Source noteuspto-grants-2014_06