Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243268Generated: November 2, 2026

Boron tribromide → 2-(4-Hydroxyphenyl)-6-(4-nonylphenyl)benzothiazole

https://huagongshe.com/reaction/1243268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-(4-Dodecyloxyphenyl)-6-(4-nonylphenyl)benzothiazoleHCID 21924524—
SolventDichloromethaneHCID 6344—
Product2-(4-Hydroxyphenyl)-6-(4-nonylphenyl)benzothiazoleHCID 13576177977.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Boron tribromide (0.53 cm3, 5.65×10−3 mol) was added dropwise to a cooled (0° C.) stirred solution of 2-(4-dodecyloxyphenyl)-6-(4-nonylphenyl)benzothiazole (2.25 g, 3.76×10−3 mol) in dichloromethane (100 cm3). The reaction mixture was stirred at room temperature overnight, then poured onto an ice/water mixture (200 g) and stirred (30 min). The reaction mixture was extracted with dichloromethane (2×75 cm3) and the combined organic layers were washed with brine (2×100 cm3) and dried (MgSO4). After filtration the solvent was removed under reduced pressure and the residue was purified by column chromatography [silica gel, ethyl acetate:hexane 1:1] followed by recrystallisation from ethyl acetate to yield 1.25 g (77.3%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07118787B2
Source datasetuspto-grants-2006_10
ORD IDord-33520a08346448e58f6074d2f382d4e6
Source noteuspto-grants-2006_10