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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286177Generated: November 1, 2026

Acetic Anhydride → HCID 20542090, compound

https://huagongshe.com/reaction/2286177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 20542075HCID 20542075—
SolventPyridineHCID 1049—
ProductHCID 20542090HCID 20542090—

Reaction Steps

A solution of 2.5 g (7.34 mmol) of 5-(o-fluorophenyl)-1,3-dihydro-7-(1-hydroxyethyl)-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one in 10 ml of acetic acid anhydride and 10 ml of pyridine is left to stand at room temperature for 24 hours and then concentrated in vacuo. The residue is taken up in chloroform and the organic phase is washed successively with 2 N hydrochloric acid, 2 N sodium bicarbonate solution and water, dried and evaporated. The residue is chromatographed on 50 g of silica gel using chloroform as the elution agent. There is obtained 1-[5-(o-fluorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]ethyl acetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327026
Source datasetuspto-grants-1982_04
ORD IDord-d9087cb3f4c042dab20d7fb5e47859e0
Source noteuspto-grants-1982_04