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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369750Generated: October 30, 2026

2-Nitrophenyl selenocyanate → rel-(3S,5S)-trans-7-Chloro-5-(2-cyclopropylethenyl)-1,5-dihydro-3-ethenyl-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-one

https://huagongshe.com/reaction/369750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrophenyl selenocyanateHCID 103931—
ReactantSodiumHCID 5360545—
Reactantrel-(3S,5S)-trans-3-(2-Bromoethyl)-7-chloro-5-cyclopropylethenyl-1,5-dihydro-5-(trifluoromethyl)-4,1-benzoxazepin-2 (3H)-oneHCID 86755964—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Productrel-(3S,5S)-trans-7-Chloro-5-(2-cyclopropylethenyl)-1,5-dihydro-3-ethenyl-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-oneHCID 6692322858.5%

Reaction Steps

To a room temperature solution of 238 mg (1.05 mmol) of 2-nitrophenylselenocyanate in 3.0 mL of THF was added 9 mL of ethanol and 66 mg of sodium borchydride. After stirring 1.5 h, a solution of 153 mg of rel-(3S,5S)-trans-3-(2-bromoethyl)-7-chloro-5-cyclopropylethenyl-1,5-dihydro-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-one in 1.5 mL of dry THF and 5 mL of ethanol was added, and the resulting mixture was stirred at ambient temperature for 32 h. The reaction mixture was partitioned between water and ether, and the organic layer was washed with aqueous bicarbonate and brine, dried and evaporated. The crude product was purified by column chromatography over silica gel (elution with 10-25% ethyl acetate in hexanes) to give 73 mg of the title compound as a pure solid which can be recrystallized from ethanol-hexanes: mp 165.5-166.5°; HRMS Calcd. for C17H16NO2F3Cl (M+H)+ : 358.082166. Found: 358.081658.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140320
Source datasetuspto-grants-2000_10
ORD IDord-1968773e180641519c140450cf99f295
Source noteuspto-grants-2000_10