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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273365Generated: October 31, 2026

Azobisisobutyronitrile → HCID 86666344, compound

https://huagongshe.com/reaction/2273365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantStyreneHCID 7501—
ReactantHCID 66884071HCID 66884071—
SolventTolueneHCID 1140—
ProductHCID 86666344HCID 86666344—

Reaction Conditions

Temperature60 °C

Reaction Steps

0.78 g (1.71 mmol, 1 eq.) of freshly prepared (4-vinylbenzyl)-bis(2,4,6-trimethylbenzoyl)-phosphine (example 1) and 1.8 mL (1.6 g, 15.4 mmol, 9 eq.) styrene are dissolved in 0.6 mL toluene. 47.6 mg (2% w/w) AIBN are added and the solution is stirred at 60° C. for 50 hours. 5 ml Toluene are subsequently added to the yellow gel which is formed in order to dissolve the polymer. The polymer is then precipitated by the addition of petroleum ether. This procedure is repeated twice before the polymer is filtrated off and washed with petroleum ether. The polymer is dried under vacuum providing 2.121 g of the (4-vinylbenzyl)-bis(2,4,6-trimethylbenzoyl)-phosphine/styrene co-polymer. Conversion: 87.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120900B2
Source datasetuspto-grants-2015_09
ORD IDord-7dbbb212ce5f4347935cbbced3fa79f3
Source noteuspto-grants-2015_09