HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264787Generated: October 23, 2026
Ethyl Acrylate → Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate
https://huagongshe.com/en/reaction/264787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Iodo-6-methylpyridin-3-ol | HCID 89957 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate | HCID 131720091 | — |
Reaction Steps
To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646286 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-50a5a9278ade4cedb4d1758badb8b7db |
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| Source note | uspto-grants-1997_07 |
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