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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220337Generated: October 30, 2026

Boron tribromide → 4-Hydroxybenzothiazole

https://huagongshe.com/reaction/2220337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant4-Methoxy-1,3-benzothiazoleHCID 12631858—
SolventDichloromethaneHCID 6344—
Product4-HydroxybenzothiazoleHCID 81901156.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

Boron tribromide (3.09 ml, 1M solution in DCM, 3.09 mmol) was added dropwise at 0° C. to a stirred solution of 4-methoxy-benzothiazole (510 mg, 3.09 mmol) in dry DCM (30ml). The resulting solution was warmed to 40° C. and allowed to stir overnight. The resulting solution was concentrated in vacuo and diluted with water and HCl (2N). The aqueous phase was neutralised to pH˜7 with NaHCO3 and the solution extracted with EtOAc (3×100 ml) and the combined organic extracts dried (MgSO4) and the solvent removed in vacuo. The resulting oil was purified by flash chromatography eluting silica gel with hexane:EtOAc [4:1] to hexane:EtOAc [7:3] to give the title compound as a tan solid (730 mg, 80%); δH (300 MHz, CDCl3) 7.59 (1H, s, CH), 7.46 (1H, dd, Ar), 7.36 (1H, t, Ar), 7.02 (1H, dd, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417064B2
Source datasetuspto-grants-2008_08
ORD IDord-a6f910b2831040b380d7ef2b23800210
Source noteuspto-grants-2008_08