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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389817Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 20295645, compound

https://huagongshe.com/reaction/1389817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 178516819HCID 178516819—
ProductHCID 20295645HCID 2029564580%

Reaction Steps

A 9.5-g (0.027 mole) portion of 7-bromo-5-(2-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one 4-oxide was added portion-wise to 50 ml of trifluoroacetic anhydride, and the reaction mixture was stirred for 90 minutes. The suspended solid that formed was collected on a filter, washed thoroughly with pentane and dried in a vacuum over KOH. There was obtained 9.72 g (80%) of 7-bromo-5-(2-fluorophenyl)-1,3-dihydro-3-trifluoroacetoxy-2H-1,4-benzodiazepin-2-one as an off-white crystalline powder: mp 175°-177° (dec.); 19F nmr (DMSO-d6) δ -74.6 ppm (s, 3F) and -112.7 ppm (m, 1F); 1H nmr (DMSO-d6) δ 6.34 ppm (s, 1H), 7.1-8.1 ppm (m, 7H), 11.5 ppm (NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246270
Source datasetuspto-grants-1981_01
ORD IDord-deb05ca0e0e2480eac6b6b92ae539fd5
Source noteuspto-grants-1981_01