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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086622Generated: October 25, 2026

Methyl 2-chloroacrylate → HCID 11034029, compound

https://huagongshe.com/reaction/1086622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-chloroacrylateHCID 6659—
ReactantTriethylamineHCID 8471—
Reactant5(2H)-Oxazolone, 4-(4-chlorophenyl)-2-(trifluoromethyl)-HCID 11065291—
SolventAcetonitrileHCID 6342—
ProductHCID 11034029HCID 1103402950.3%

Reaction Steps

Triethylamine (5.58 g, 0.055 mol) is added dropwise to a mixture of 4-(p-chlorophenyl)-2-(tri-fluoromethyl)-5(2H)-oxazolone (15.6 g, 0.054 mol), methyl α-chloroacrylate (6.52. g, 0.054 mol) and acetonitrile (50 mL). The reaction mixture heats up to 55° C. during the addition. After the addition is complete, the reaction mixture is heated at reflux temperature for one hour, cooled to room temperature and filtered. The filtrate is poured into an ether/water mixture and extracted with ether. The combined organic extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to give a black residue. Recrystallization of the residue from hexane gives the title compound as an orange solid (8.25 g, 50.2%). Indentified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030735
Source datasetuspto-grants-1991_07
ORD IDord-54aa8239b4884d85ac93d6770a8f831e
Source noteuspto-grants-1991_07