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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ethyl 7-chloro-2,3-dihydro-2-oxo-5-phenyl-1H-1,4-benzodiazepine-3-carboxylate | HCID 110682 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 10-chloro-11b-phenyl-2,3,5,11b-tetrahydrooxazolo[3,2-d] [1,4]benzodiazepin-6(7H)-one-5-carboxylic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04049666 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-a1eb78922a364c139d40e9acf1e50940 |
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| Source note | uspto-grants-1977_09 |
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