HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379252Generated: October 25, 2026
Triethylamine → Ethyl 3-(6-methoxy-3-pyridyl)acrylate
https://huagongshe.com/reaction/379252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 5-Bromo-2-methoxypyridine | HCID 2734895 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 3-(6-methoxy-3-pyridyl)acrylate | HCID 53930754 | — |
Reaction Steps
A solution of the 5-bromo-2-methoxypyridine 16-2 (74.3 g, 0.4 mol), ethyl acrylate (150 mL, 1.4 mol), triethylamine (150 mL, 1.08 mol), palladium acetate (10 g, 0.045 mol) and tri-o-tolylphosphine (20 g, 0.066 mol) in 100 mL acetonitrile was degassed with argon for 10 minutes. The mixture was heated at 90° C. for 12 hr, then the volatiles were removed in vacuo. Toluene (300 mL) was added and the mixture concentrated again. Diethyl ether (300 mL) was added and the mixture filtered through a pad of silica gel eluting with 800 mL of diethyl ether. After removal of the diethyl ether, the residue was chromatographed on silica gel eluting with EtOAc/hexane, 1:19 then 1:14 then 1:9 to give 16-3 as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297249B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-d62bc6c0881343ef8e9df67de26e597e |
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| Source note | uspto-grants-2001_10 |
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