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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7737Generated: October 26, 2026

Carbon Tetrachloride → Benzoxazole

https://huagongshe.com/reaction/7737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(3,5-Dimethoxy-4-methylphenyl)-1,3-benzoxazoleHCID 21990974—
SolventEthyl AcetateHCID 8857—
ProductBenzoxazoleHCID 9228—

Reaction Steps

A mixture of 2-(3,5-dimethoxy-4-methylphenyl)-1,3-benzoxazole (260 mg, 1 mmol), carbon tetrachloride (4.2 mL), benzoyl peroxide (15 mg, 0.06 mmol) and N-bromosuccinimide (270 mg, 1.5 mmol) was heated to reflux conditions under argon overnight. Concentration of cooled reaction mixture in vacuo afforded a yellow solid. Flash chromatography on silica gel of crude material using 1:4 EtOAc:hexanes gave the desired intermediate, 2-[4-bromomethyl)-3,5-dimethoxyphenyl]-1,3-benzoxazole, as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087601B2
Source datasetuspto-grants-2006_08
ORD IDord-394150f62b5b4dda8aa07bbea70ff52f
Source noteuspto-grants-2006_08