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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867061Generated: October 31, 2026

Triphenylphosphine → 2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepine

https://huagongshe.com/reaction/867061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-(2-Azido-1-ethoxyethylideneamino)-5-nitrobenzophenoneHCID 20317263—
SolventBenzeneHCID 241—
Product2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepineHCID 20317264—

Reaction Steps

To a solution of 2.5 parts of 2-(2-azido-1-ethoxyethylideneamino)-5-nitrobenzophenone produced in Step (2) in 30 parts by volume of benzene is added with stirring 1.78 parts of triphenylphosphine. The mixture is stirred for further 1.5 hours and the solvent is removed by distillation. The residue is extracted with a mixture of n-hexane and acetone (7:3), and the soluble fraction is purified by means of chromatography employing Silica Gel, whereupon 2-ethoxy-7-nitro-5-phenyl-3H-1,4-benzodiazepine is obtained as pale yellow crystals. Recrystallization from ether-n-hexane gives pale yellow prisms melting at 143°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04102881
Source datasetuspto-grants-1978_07
ORD IDord-e605eaf53e8a4d72bd3be540b5d972d5
Source noteuspto-grants-1978_07