HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668276Generated: November 1, 2026
tert-Butyl methacrylate → t-Butyl methacrylate 4-vinylquinoline 4-acetoxystyrene
https://huagongshe.com/reaction/1668276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methacrylate | HCID 11448 | — |
| Reactant | 1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate) | HCID 75763 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 4-Ethenylquinoline | HCID 13319577 | — |
| Solvent | Cyclohexanone | HCID 7967 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | t-Butyl methacrylate 4-vinylquinoline 4-acetoxystyrene | HCID 86629094 | 299.6% |
Reaction Steps
4-Acetoxystyrene (29.19 g) (0.18 mol), 12.80 g (0.09 mol) of t-butyl methacrylate, 4.66 g (0.03 mol) of 4-vinylquinoline, and 3.45 g (0.015 mol) of polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries) are dissolved in 148.99 g of cyclohexanone. Cyclohexanone (37.25 g) is put in a reaction vessel and the above solution is dropped into the reaction system at 80° C. over 6 hours under nitrogen gas atmosphere. After dropping, the reaction solution is stirred while heating for 2 hours, and then allowed to cool to room temperature. The solution is dropped into 2.5 liters of hexane to thereby precipitate and filter the polymer. The solid filtered is roughly washed with 500 ml of hexane and dried under reduced pressure to obtain 41.30 g of t-butyl methacrylate/4-vinylquinoline/4-acetoxystyrene copolymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989137B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-ff772c5ce1d44ddb8c9cd9f6dbc6d075 |
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| Source note | uspto-grants-2011_08 |
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