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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973070Generated: October 26, 2026

Ammonia → RO-05-2921

https://huagongshe.com/reaction/1973070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantFormaldehydeHCID 712—
ReactantN-(2-benzoylphenyl)-2-chloroacetamideHCID 2064069—
SolventMethanolHCID 887—
ProductRO-05-2921HCID 7617584.7%

Reaction Steps

Paraformaldehyde (200 g., 91% flake) is placed in a stirred reactor equipped with a reflux condenser, decanter, and ammonia addition tube. Methanol (575 mls.) is added and then gaseous ammonia below the surface of the reaction mixture. 2-Chloroacetamido-benzophenone (273.7 g.) is then added. With a slow, continuous flow of ammonia to the reaction zone, the mixture is heated at reflux for 5 hours. The crystal slurry obtained is distilled to recover the methanol. Toluene (1350 mls.) is now added to the crystal residue and residual water is removed by azeotropic distillation through the decanter. When dry, the hot toluene solution is filtered, the filtrate is cooled for crystallization, and the product obtained isolated to give 1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one (200 g., 84.7%) m.p. 180°-181° C. (uncorr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996209
Source datasetuspto-grants-1976_12
ORD IDord-4caa97eb1a444f299db8130eb2318f7b
Source noteuspto-grants-1976_12