HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902575Generated: October 28, 2026
Methyl Acrylate → methyl (E)-3-(3-quinolinyl)-2-propenoate
https://huagongshe.com/reaction/902575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | methyl (E)-3-(3-quinolinyl)-2-propenoate | HCID 1491214 | — |
Reaction Steps
In an amount of 10.2 g of 3-bromoquinoline was stirred together with 7 ml of methyl acrylate, 110 mg of palladium(II) acetate, 599 mg of tri-o-tolylphosphine, and 29 ml of triethylamine at 100° C. for 17 hours in a sealed tube. The reaction mixture was diluted with 300 ml of chloroform, and successively washed with 250 ml of saturated brine, and 250 ml of saturated aqueous ammonium chloride. The organic layer was dried over anhydrous sodium sulfate, and then filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was dissolved in 80 ml of chloroform, added with 200 ml of hexane under ice cooling, and stirred for 30 minutes. The precipitates were taken by filtration, washed with hexane, and then dried under reduced pressure to obtain 8.0 g of methyl (E)-3-(quinolin-3-yl)acrylate. Physicochemical Properties of this Compound
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365174B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-a5cbe1bea1f141bd98df28de0a72be4a |
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| Source note | uspto-grants-2008_04 |
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