HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086622Generated: October 25, 2026
Methyl 2-chloroacrylate → HCID 11034029, compound
https://huagongshe.com/reaction/1086622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-chloroacrylate | HCID 6659 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5(2H)-Oxazolone, 4-(4-chlorophenyl)-2-(trifluoromethyl)- | HCID 11065291 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11034029 | HCID 11034029 | 50.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05030735 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-54aa8239b4884d85ac93d6770a8f831e |
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| Source note | uspto-grants-1991_07 |
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