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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975226Generated: October 27, 2026

Azobisisobutyronitrile → HCID 57254888, compound

https://huagongshe.com/reaction/1975226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHexadecanethiolHCID 18015—
Reactant3,3'-((2,2-Bis((allyloxy)methyl)-1,3-propanediyl)bis(oxy))dipropeneHCID 73855—
ProductHCID 57254888HCID 57254888—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 250 ml three-necked flask equipped with a magnetic stirrer, a condenser and a nitrogen inlet tube was first purged with nitrogen 107 grams of n-hexadecyl mercaptan (0.417 mole) was then charged and heated to 80° C. To the heated and stirred n-hexadecyl mercaptan, a solution of 0.2 gram of 2,2'-azobis(isobutyronitrile) in 29.64 grams (0.1 mole) of pure pentaerythritol tetraallyl ether was added dropwise over a 15-minute period. One-half hour after this addition was completed, 0.1 gram of 2,2'-azobis(isobutyronitrile) was added. Two more 0.1 gram additions of 2,2'-azobis-(isobutyronitrile) were made at half-hour intervals. After the last addition, the reaction was held at 80° C. for an additional hour. The crude product was recrystallized three times in 300 ml. of hexane yielding 57 grams of a white solid having a melting point of 55°-57° C. The elemental analysis found: C - 73.4%, H - 11.9%, S(total) - 10.0%, and S(mercapto) - 3 ppm. Calculated for C98H164S2 ; C - 73.12%, H-12.43%, S(total) - 9.64% and S(mercapto) - 4 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284886
Source datasetuspto-grants-1994_02
ORD IDord-e02f9d242db54acb9ec70d4a4ec2bc17
Source noteuspto-grants-1994_02