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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438015Generated: November 1, 2026

4-Methoxybenzyl bromide → HCID 57941459, compound

https://huagongshe.com/reaction/1438015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl bromideHCID 165021—
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 57941459HCID 5794145978%

Reaction Conditions

Temperature80 °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; 150 mg, 0.49 mmol), tetrabutylammonium iodide (181 mg, 0.49 mmol) and 4-methoxybenzyl bromide (280 μL, 1.94 mmol) in dimethylformamide (3 mL) was heated at 80° C. overnight. The solvent was evaporated, dichloromethane (50 mL) was added and the solution was washed with water (2×20 mL), saturated aqueous sodium thiosulfate (20 mL), and brine (20 mL). The solution was dried (magnesium sulfate), filtered, evaporated, and purified by column chromatography, eluting with 60-75% ethyl acetate/petroleum ether, and dried under high vacuum overnight to give (4S,7R)-2-(2,4-difluoro-phenyl)-1-(4-methoxy-benzyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (162 mg, 78%). APCI(+)-MS (M+H) 425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-35962af6a2494a939eea977f88da829c
Source noteuspto-grants-2009_11