HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705995Generated: October 27, 2026
Water → 3-(2-Methoxy-pyridin-4-yl)-acrylic acid methyl ester
https://huagongshe.com/reaction/705995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | 2-Methoxypyridine-4-carbaldehyde | HCID 2762996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Methoxy-pyridin-4-yl)-acrylic acid methyl ester | HCID 67775125 | 92.3% |
Reaction Steps
To a solution of 2-Methoxy-pyridine-4-carbaldehyde (1 g, 7.29 mmol, 1 eq) in 50 ml of dry DCM was added portionwise (methoxycarbonylmethylene)triphenylphosphorane (1.05 eq, 2.56 g). The mixture was stirred at room temperature for 2 hours. The mixture was then poured into 200 ml of water and the organic substances were extracted with DCM (twice, 150 ml of DCM was used in total) The gathered DCM layers were dried and the resulting crude was purified by chromatography on BIOTAGE SP1 purification device using 50 g normal phase silica SNAP coloumn and cyclohexane/EtOAc solvent system (gradient 2-20% of EtOAc in 20 coloumn volumes). Solvent from the gathered fractions of appropriate composition was evaporated and obtained was 3-(2-methoxy-pyridin-4-yl)-acrylic acid methyl ester (1.3 g, yield=87.6%, purity=95%). MS: [M+H]+=194.14 1H NMR (300 MHz; CDCl3) δ/ppm 3.82 (s, 3H), 3.95 (s, 3H), 6.54 (d, J=16.0 Hz, 1H), 6.80 (s, 1H), 6.97 (dd, J=5.38 Hz, J=1.31 Hz, 1H), 7.55 (d, J=16.0 Hz, 1H), 8.18 (d, J=5.38 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09174968B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-f822eaf9b9da4a2884a7e7c877d2684a |
|---|
| Source note | uspto-grants-2015_11 |
|---|