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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735433Generated: October 31, 2026

Water → 4-(2-cyclopentyl-7-fluoro-2H-indazol-3-yl)phenol

https://huagongshe.com/reaction/735433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclohexeneHCID 8079—
ReactantBoron tribromideHCID 25134—
Reactant2-cyclopentyl-7-fluoro-3-(4-methoxyphenyl)-2H-indazoleHCID 11500562—
SolventDichloromethaneHCID 6344—
Product4-(2-cyclopentyl-7-fluoro-2H-indazol-3-yl)phenolHCID 13545396457.2%

Reaction Steps

A solution of 2-cyclopentyl-7-fluoro-3-(4-methoxyphenyl)-2H-indazole (0.055 g, 0.177 mmol) in CH2Cl2 containing excess equivalents of cyclohexene (0.3 mL) at −78° C. was treated with boron tribromide (0.70 mL, 0.74 mmol, 4 eq.) and slowly allowed to warm to ambient temperature. The reaction mixture was quenched by dropwise addition of CH3OH to the cooled reaction mixture. The solvent was removed in vacuo and the residue partitioned with EtOAc and 1 N HCl. The organic phase was washed with brine and dried (Na2SO4). Removal of the solvent in vacuo afforded the crude product. Pure product was obtained by crystallization or flash chromatography through water deactivated silica gel to give the product (0.03 g) as an amber solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592363B2
Source datasetuspto-grants-2009_09
ORD IDord-76d38e7eb9f74ed18332b4ace7d15f51
Source noteuspto-grants-2009_09