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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071962Generated: October 29, 2026

Ethylene Oxide → 10-chloro-11b-phenyl-2,3,5,11b-tetrahydrooxazolo[3,2-d] [1,4]benzodiazepin-6(7H)-one-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2071962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantAmmonium HydroxideHCID 14923—
ReactantEthyl 7-chloro-2,3-dihydro-2-oxo-5-phenyl-1H-1,4-benzodiazepine-3-carboxylateHCID 110682—
Solvent1,2-DichloroethaneHCID 11—
Product10-chloro-11b-phenyl-2,3,5,11b-tetrahydrooxazolo[3,2-d] [1,4]benzodiazepin-6(7H)-one-5-carboxylic acid ethyl esterHCID 53917092—

Reaction Steps

To a solution of 3.1 g. (0.0118 M) of stannic chloride in 35 ml of dry ethylene dichloride under nitrogen was added 1.5 g. (0.00438 M) of 7-chloro-1,3-dihydro-2-oxo-5-phenyl-2H-1,4-benzodiazepine-3-carboxylic acid ethyl ester. The reaction was stirred in an ice bath, when a solution of 1.0 g. (0.0233 M) of ethylene oxide in 5 ml. of ethylene dichloride was added. The mixture was stirred at room temperature for 3 hr. and then made basic with mixture of ammonium hydroxide and ice. The mixture was filtered, and the filtrate was dried with anhydrous sodium sulfate and evaporated to dryness. The residue was crystallized from ether. Recrystallization from a mixture of dichloromethane and petroleum ether gave 10-chloro-11b-phenyl-2,3,5,11b-tetrahydrooxazolo[3,2-d] [1,4]benzodiazepin-6(7H)-one-5-carboxylic acid ethyl ester as white rods, m.p. 205°-207°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049666
Source datasetuspto-grants-1977_09
ORD IDord-a1eb78922a364c139d40e9acf1e50940
Source noteuspto-grants-1977_09