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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438023Generated: November 2, 2026

1-(Bromomethyl)-3-fluoro-5-(trifluoromethyl)benzene → HCID 57941435, compound

https://huagongshe.com/reaction/1438023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-3-fluoro-5-(trifluoromethyl)benzeneHCID 2737575—
Reactant(4s,7r)-2-(2,4-Difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-oneHCID 57941339—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 57941435HCID 5794143554.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (4S,7R)-2-(2,4-difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 14; 25 mg, 0.08 mmol), tetrabutylammonium iodide (30 mg, 0.08 mmol) and 3-fluoro-5-trifluoromethyl-benzyl bromide (75 mg, 0.29 mmol) in dimethylformamide (1 mL) was heated at 100° C. overnight. The reaction mixture was diluted with dichloromethane (50 mL) and the solution was washed with water/brine (1:1; 20 mL), water (2×20 mL), sodium thiosulfate (20 mL) and brine (20 mL). The solution was dried (magnesium sulfate), filtered, concentrated and purified by chromatography, eluting with 50% ethyl acetate/petroleum ether, to give (4S,7R)-2-(2,4-difluoro-phenyl)-1-(3-fluoro-5-trifluoromethyl-benzyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (21 mg, 53%) as an off-white solid. APCI(+)-MS (M+H) 481.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-5f864119c339434f86d142b682821f77
Source noteuspto-grants-2009_11