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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735923Generated: October 31, 2026

p-Anisoyl chloride → 4-methacryloyloxybutyl (E)-3-[4-(4-methoxyphenylcarbonyloxy)phenyl]acrylate

https://huagongshe.com/reaction/1735923

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant4-methacryloyloxybutyl (E)-3-(4-hydroxyphenyl)acrylateHCID 22077725—
SolventDichloromethaneHCID 6344—
Product4-methacryloyloxybutyl (E)-3-[4-(4-methoxyphenylcarbonyloxy)phenyl]acrylateHCID 6757045089.2%

Reaction Steps

2.0 g of 4-methoxybenzoyl chloride in 25 ml of dichlormethane were added dropwise at 0° C. while stirring within 30 min. to a solution of 3.5 g of 4-methacryloyloxybutyl (E)-3-(4-hydroxyphenyl)acrylate and 1.2 g of triethylamine in 40 ml of dichloromethane. The reaction mixture was stirred at room temperature overnight, then filtered and subsequently concentrated. Chromatographic purification of the residue on silica gel with hexane/ethyl acetate (vol. 7:3) and two-fold recrystallization from ethanol gave 4.5 g of 4-methacryloyloxybutyl (E)-3-[4-(4-methoxyphenylcarbonyloxy)phenyl]acrylate, m.p. 89°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539074
Source datasetuspto-grants-1996_07
ORD IDord-aa56edd608ce46dba02aba381392694e
Source noteuspto-grants-1996_07