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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438025Generated: November 2, 2026

Ethanol → HCID 57941431, compound

https://huagongshe.com/reaction/1438025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDichloromethaneHCID 6344—
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
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—
ProductHCID 57941431HCID 5794143173.1%

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; 100 mg, 0.33 mmol), tetrabutylammonium iodide (120 mg, 0.32 mmol) and 3,5-bis(trifluoromethyl)benzyl bromide (240 μL, 1.3 mmol) in dimethylformamide (2 mL) was heated at 100° C. overnight. Dichloromethane (50 mL) was added and the solution was washed with 1:1 water/brine (20 mL), water (2×20 mL), aqueous sodium thiosulfate (20 mL), and brine (20 mL). The solution was dried (magnesium sulfate), filtered, evaporated, and purified by column chromatography, eluting with 45-50% ethyl acetate/petroleum ether, to give an oil. The oil was co-evaporated with ethanol, and the residue was held under high vacuum to give (4S,7R)-1-(3,5-bis-trifluoromethyl-benzyl)-2-(2,4-difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (128 mg, 73%) as a white solid. APCI(+)-MS (M+H) 531.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-282f0a42f2724a24a8cb19bc0041738d
Source noteuspto-grants-2009_11