Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528561Generated: November 3, 2026

Azobisisobutyronitrile → HCID 86712493, compound

https://huagongshe.com/reaction/1528561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86712494HCID 86712494—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 86712493HCID 86712493—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2-(2,5-bis(hexyloxy)-4-(4-methylbenzo[d]oxazol-2-yl)phenyl)-5-(tert-butyl)benzo[d]oxazol (3.7 g, 6.35 mmol), N-bromosuccinimide (NBS) (1.13 g, 6.35 mmol), and AIBN (0.1 g, 0.6 mmol) in CCl4 (40 mL) was heated to reflux for 15 h under dry argon atmosphere. The reaction mixture was cooled to 0° C. and the precipitate was removed by filtration while maintaining the temperature at 0° C. After the solvent was evaporated, 4-(bromomethyl)-2-(4-(5-(tert-butyl)benzo[d]oxazol-2-yl)-2,5-bis(hexyloxy)phenyl)benzo[d]oxazole was obtained as an oil, which was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090602B2
Source datasetuspto-grants-2015_07
ORD IDord-3fb6720d529941a9a54bb7b80a96e9f9
Source noteuspto-grants-2015_07