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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635022Generated: November 2, 2026

4-Bromo-1,1,1-trifluorobutane → HCID 22392982, compound

https://huagongshe.com/reaction/1635022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1,1,1-trifluorobutaneHCID 521006—
ReactantBenzyl (2-oxo-5-phenyl-2,3-dihydro-1h-benzo[e][1,4]diazepin-3-yl)carbamateHCID 2756242—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 22392982HCID 22392982—

Reaction Steps

To a solution of 3-(benzoxycarbonyl)amino-2,3-dihydro-5-phenyl-1H-1,4-benzodiazepin-2-one (3.7 g, 9.61 mmol) in 40 mL of anhydrous DMF at 0° C. was added potassium tert-butoxide (1.6 g, 14.4 mmol) in one portion. The reaction mixture was stirred 20 m. and 4,4,4-trifluoro-1-bromobutane (Lancaster; Windham, N.H.; 2.6 g, 13.4 mmol) was added. The reaction mixture was warmed to room temperature over 30 min. and the n diluted with 100 mL of water and 200 mL of methylene chloride. The layers were separated. The organic layer was extracted with water and dried over sodium sulfate. Purification of the crude product by silica gel column chromatography (0-3% ethyl acetate/methylene chloride) gave 1.52 g (32%) of an off white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509331B1
Source datasetuspto-grants-2003_01
ORD IDord-1a3670bed14a4ae69d6ef2a948be86f7
Source noteuspto-grants-2003_01