HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488881Generated: November 1, 2026
Methyl Acrylate → HCID 10210567, compound
https://huagongshe.com/reaction/488881
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 22267230 | HCID 22267230 | — |
| Catalyst | Palladium (II) acetate | HCID 4144353 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10210567 | HCID 10210567 | 67% |
Reaction Steps
A solution of 2-[4-(3-bromophenyl)-7-chloro-6-methyl-2-oxo-2H-chromene-3-yl]-N-[4-chloro-2-(trifluoromethyl)phenyl]acetamide (500 mg) in DMF (5 ml) was combined with methyl acrylate (0.14 ml), triethylamine (0.21 ml), pd(OAc)2 (5 ml) and triphenylphosphine (10 mg) under argon atmosphere, and heated at 120° C. for 3 hours. After the reaction was completed, the mixture was combined with water, and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate, and then concentrated. The resultant residue was purified by a silica gel chromatography (eluent: hexane-ethyl acetate=2:1), and then recrystallized from THF-ethyl acetate to obtain the title compound as a colorless crystal (333 mg, yield: 67%). Melting point: 202-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974806B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-a5b46a8ff36a49a4a23ed08eeea91850 |
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| Source note | uspto-grants-2005_12 |
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