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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283338Generated: October 31, 2026

Methanol → 1-(beta-Hydroxy-ethyl)-5-phenyl-7-chloro-1H-1,5-benzodiazepine-2,4-(3H,5H)-dione

https://huagongshe.com/reaction/1283338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthylene OxideHCID 6354—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantDesmethylclobazamHCID 89657—
SolventWaterHCID 962—
Product1-(beta-Hydroxy-ethyl)-5-phenyl-7-chloro-1H-1,5-benzodiazepine-2,4-(3H,5H)-dioneHCID 21517175—

Reaction Steps

A mixture consisting of 28.6 gm (0.1 mol) of 5-phenyl-7-chloro-1H-1,5-benzodiazepine-2,4-(3H,5H)-dione, 500 ml of methanol, 25 ml of water, 10-15 ml of ethyleneoxide and 1 ml of Triton B (methanolic 35% solution of benzyl trimethylammonium hydroxide) was stirred at room temperature for about eight hours. Thereafter, the clear solution formed thereby was evaporated, the residue was taken up in methylene chloride, and the resulting solution was extracted with water, dried and evaporated. The residue was recrystallized from ethanol, yielding 25.6 gm (78% of theory) of the colorless crystalline compound of the formula ##SPC6##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE028935
Source datasetuspto-grants-1976_08
ORD IDord-52a45b361d134fbdbe957583f0861db4
Source noteuspto-grants-1976_08