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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633503Generated: October 29, 2026

Acetic Anhydride → HCID 18679315, compound

https://huagongshe.com/reaction/1633503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant7-Chloro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepineHCID 21853965—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18679315HCID 1867931522.6%

Reaction Steps

7-chloro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine (12.5 mmol) was dissolved in a mixture of THF (100 mL), Et3N (19.1 mmol) and acetic anhydride (12.4 mmol). The reaction mixture was heated under reflux for 18 h, cooled to room temperature and partitioned between H2O and EtOAc. The aqueous phase was extracted again 2× with EtOAc and the combined organic layers were dried over MgSO4, filtered and concentrated to a yellow, oily solid. The crude material was purified by column chromatography on silia eluting with EtOAc to yield 3-acetyl-7-chloro-1,2,3,5-tetrahydro-4H-[1,4]benzodiazepine (2.8 mmol, 22%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503900B2
Source datasetuspto-grants-2003_01
ORD IDord-5a6415343520435fad93957b43e8418c
Source noteuspto-grants-2003_01