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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442323Generated: October 26, 2026

Menthyl chloroformate → 1methyl-4-menthyloxycarbonyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one

https://huagongshe.com/reaction/442323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMenthyl chloroformateHCID 151928—
Reactant4,5-DihydrodiazepamHCID 3081984—
ReactantMagnesium monoxideHCID 6850729—
SolventAcetoneHCID 180—
Product1methyl-4-menthyloxycarbonyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-oneHCID 68125163—

Reaction Steps

0.2 g. of magnesium oxide and 1.21 g. (0.0055 moles) of menthyloxycarbonyl chloride are added to a solution of 1.34 g. (0.005 moles) of 1-methyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one in 20 ml. of acetone, and the mixture is stirred overnight. Next day carbon is added to the mixture, the suspension is filtered, and the filtrate is evaporated to dryness. The oily residue is dissolved in 20 ml. of ethyl acetate, the solution is shaken with 3×5 ml. of 0.1 N hydrochloric acid, the organic phase is washed with water until neutral, then dried over sodium sulfate. The drying agent is filtered off, and the filtrate is evaporated. The residue is admixed with hexane, and the solids are filtered off. 0.82 g. of 1methyl-4-menthyloxycarbonyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one, melting at 144°- 144.5° C., are obtained. The obtained substance is recrystallized from a mixture of ethanol and water. Rf2 = 0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045433
Source datasetuspto-grants-1977_08
ORD IDord-8b4e3b0c2dd449fc9ac6ee7e2f96066b
Source noteuspto-grants-1977_08