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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582294Generated: November 1, 2026

Azobisisobutyronitrile → 5-(Bromomethyl)benzo[d]oxazole

https://huagongshe.com/reaction/1582294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-MethylbenzoxazoleHCID 2724970—
SolventCarbon TetrachlorideHCID 5943—
Product5-(Bromomethyl)benzo[d]oxazoleHCID 2198498139.6%

Reaction Steps

A mixture of 5-methylbenzoxazole (200 mg, 1.50 mmol), N-bromosuccinimide (321 mg, 1.80 mmol), and 2,2′-azobisisobutyronitrile (37 mg, 0.23 mmol) in CCl4 (3 mL) was heated at reflux for 22 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. Purification of the crude material on silica gel (5% EtOAc/hexanes) gave the title compound as a colourless crystals (126 mg, 39%). 1H NMR (CDCl3) δ4.64 (s, 2H), 7.46 (dd, 1H, J=8.6, 1.7 Hz), 7.57 (d, 1H, J=8.4 Hz), 7.83 (d, 1H, J=1.2 Hz), 8.12 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-e2b3201e5d5b400d97c6fa5759726451
Source noteuspto-grants-2004_05