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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062232Generated: November 1, 2026

Boron tribromide → 2-(4-Chloro-7-methylquinazolin-2-yl)-3-methylphenol

https://huagongshe.com/reaction/2062232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant4-Chloro-2-(2-methoxy-6-methyl-phenyl)-7-methyl-quinazolineHCID 58010790—
SolventDichloromethaneHCID 6344—
Product2-(4-Chloro-7-methylquinazolin-2-yl)-3-methylphenolHCID 136121446—

Reaction Steps

To a solution of 4-chloro-2-(2-methoxy-6-methylphenyl)-7-methylquinazoline (669 mg, 2.24 mmol) in 7 mL CH2Cl2 was added dropwise 5 equivalents of a 1 M solution of BBr3 in CH2Cl2 at −78° C. The reaction was warmed to room temperature and was complete in 30 minutes. The reaction was quenched with a saturated aqueous NaHCO3 solution until the pH was neutral. The aqueous layer was extracted with CH2Cl2, dried over MgSO4, filtered, and concentrated to obtain 2-(4-chloro-7-methylquinazolin-2-yl)-3-methylphenol. LC/MS: m/z 285.1 (M+H)+ at 3.94 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283354B2
Source datasetuspto-grants-2012_10
ORD IDord-8424b88027b04c9d8b25a93d50bd985d
Source noteuspto-grants-2012_10