HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970259Generated: October 28, 2026
Azobisisobutyronitrile → HCID 23295550, compound
https://huagongshe.com/reaction/970259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 23295550 | HCID 23295550 | — |
Reaction Steps
In 400 mL of isopropanol, 84.1 g of p-hydroxystyrene, 20.8 g of styrene and 12.8 g of tert-butyl acrylate were dissolved, then 14.1 g of azobisisobutylonitrile was added and the solution reacted at 80° C. for 6 hours under nitrogen gas flow. After the reaction, said reaction liquid was poured into 10 L of water for precipitation, followed by filtering off deposited crystal, drying under reduced pressure to obtain 95 g of poly(p-hydroxystyrene/styrene/tert-butyl acrylate) as a pale brown powder crystal. The copolymer obtained was named polymer 1. A composition ratio of p-hydroxystyrene unit, styrene unit and tert-butyl acrylate unit in polymer 1 was found to be about 7:2:1 from the measurement results by 13CNMR. Weight average molecular weight (Mw) of this copolymer was about 10,000 and distribution (Mw/Mn) thereof was about 1.9 from the measurement results by gel permeation chromatography using polystyrene as a standard.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312014B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-4d7a76ef02964892b586ac7834e67453 |
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| Source note | uspto-grants-2007_12 |
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