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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methacrylateHCID 11448—
Reactant1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate)HCID 75763—
Reactant4-Ethenylphenyl acetateHCID 75821—
Reactant4-EthenylquinolineHCID 13319577—
SolventCyclohexanoneHCID 7967—
SolventHexaneHCID 8058—
Productt-Butyl methacrylate 4-vinylquinoline 4-acetoxystyreneHCID 86629094299.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989137B2
Source datasetuspto-grants-2011_08
ORD IDord-ff772c5ce1d44ddb8c9cd9f6dbc6d075
Source noteuspto-grants-2011_08