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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963483Generated: October 30, 2026

Acetic Anhydride → HCID 135829355, compound

https://huagongshe.com/reaction/963483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178516818HCID 178516818—
SolventChloroformHCID 6212—
ProductHCID 135829355HCID 135829355—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of 5-cyclohexy-2,3-dihydro-1H-1,4-benzodiazepin-2-one-4-oxide (0.70 g) in chloroform (10 ml) was added acetic anhydride (3.7 ml) at ambient temperature and the mixture was heated for 4 hours at 70° C. After cooling, the mixture was concentrated in vacuo. The residue was taken up with chloroform. The organic layer was washed with saturated aqueous sodium carbonate, dried over magnesium sulfate, filtered off and concentrated in vacuo to give a crude product. The crude product was purified by column chromatography on silica gel with chloroform to give (3RS)-3-acetoxy-5-cyclohexyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763437
Source datasetuspto-grants-1998_06
ORD IDord-3709955e13d2435090da73d74c60e87d
Source noteuspto-grants-1998_06