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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982432Generated: November 1, 2026

Azobisisobutyronitrile → 5-Bromomethyl-4-(4-chlorophenyl)-2-methyloxazole

https://huagongshe.com/reaction/1982432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantOxazole, 4-(4-chlorophenyl)-2,5-dimethyl-HCID 11160071—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromomethyl-4-(4-chlorophenyl)-2-methyloxazoleHCID 13293293—

Reaction Steps

A solution of 4-(4-chlorophenyl)-2,5-dimethyloxazole (6.21 g), N-bromosuccinimide (5.34 g) and azobisisobutyronitrile (0.25 g) in carbon tetrachloride (90 ml) was refluxed with stirring for 15 minutes, then washed with water, saturated aqueous sodium hydrogen carbonate and water in that order, and dried over anhydrous magnesium sulfate. The solvent was then distilled off and the residue was crystallized from cold ethanol to give 5-bromomethyl-4-(4-chlorophenyl)-2-methyloxazole, yield 6.73 g (78.4%). Recrystallization from ethanol gave needles, melting at 75°-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596816
Source datasetuspto-grants-1986_06
ORD IDord-39e7788ed2e845adb0303efd9a11125e
Source noteuspto-grants-1986_06