HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975226Generated: October 27, 2026
Azobisisobutyronitrile → HCID 57254888, compound
https://huagongshe.com/reaction/1975226
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Hexadecanethiol | HCID 18015 | — |
| Reactant | 3,3'-((2,2-Bis((allyloxy)methyl)-1,3-propanediyl)bis(oxy))dipropene | HCID 73855 | — |
| Product | HCID 57254888 | HCID 57254888 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05284886 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-e02f9d242db54acb9ec70d4a4ec2bc17 |
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| Source note | uspto-grants-1994_02 |
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