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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959551Generated: November 4, 2026

Boron tribromide → 4-Bromo-2-methyl-quinolin-8-ol

https://huagongshe.com/reaction/1959551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSilane, tris(1-methylethyl)-HCID 138754—
Reactant4-Bromo-8-methoxy-2-methylquinolineHCID 17750596—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2-methyl-quinolin-8-olHCID 67077159—

Reaction Steps

BBr3 (1 M in DCM, 108 mL, 108 mmol) was added dropwise to a stirred solution of 4-bromo-8-methoxy-2-methyl-quinoline (7.8 g, 31 mmol) and triisopropyl-silane (6.2 mL, 31 mmol) in anhydrous DCM (300 mL) at −80° C. The reaction mixture was allowed to warm to room temperature over 4 h. The reaction mixture was then concentrated in vacuo and the residue was partitioned between DCM (300 mL), water (50 mL), and concentrated aqueous NH3 (20 mL). The aqueous layer was extracted with DCM (2×300 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (elution with DCM/EA 10:1) to give the title compound. MS (m/z): 238.3 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410134B2
Source datasetuspto-grants-2013_04
ORD IDord-aef0d4574c224ac2aea9ee9ee1df8a22
Source noteuspto-grants-2013_04