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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196382Generated: October 29, 2026

Boron tribromide → 3-tert-butyl-6-hydroxy-2-methyl-4-phenylisoquinolin-1(2H)-one

https://huagongshe.com/reaction/2196382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-tert-butyl-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-oneHCID 68509193—
SolventDichloromethaneHCID 6344—
Product3-tert-butyl-6-hydroxy-2-methyl-4-phenylisoquinolin-1(2H)-oneHCID 11278230—

Reaction Steps

To a methylene chloride (5 mL) solution of 3-tert-butyl-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one (100 mg, 0.311 mmol) under argon at −70 C was added boron tribromide (1.0M, 0.934 mL, 0.934 mmol). The contents of the reaction flask were warmed to room temperature and stirred 24 h. Extracted with methylene chloride (3×), then the combined organic extracts were washed with brine and dried with anhydrous sodium sulfate. Filtration followed by evaporation of solvent in vacuo gave a solid which was triturated with ethanol. Recrystallization from ethyl acetate/ethanol afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338449B2
Source datasetuspto-grants-2012_12
ORD IDord-ae2339bbfa844f64909d2dddfcc2ed2f
Source noteuspto-grants-2012_12