HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232239Generated: October 29, 2026
2-Cyano-3-(4-methoxyphenyl)prop-2-enoic acid → 2-Cyano-3-(4-methoxyphenyl)propanoic acid
https://huagongshe.com/reaction/2232239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Cyano-3-(4-methoxyphenyl)prop-2-enoic acid | HCID 233260 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-Cyano-3-(4-methoxyphenyl)propanoic acid | HCID 13711148 | — |
Reaction Steps
Sodium borohydride (30.2 g) is added portionwise over a period of 2 hours to a stirred mixture of α-cyano-4-methoxycinnamic acid (52.5 g) in aqueous saturated NaHCO3 (200 ml) and methanol (600 ml) cooled to about 15° C. The reaction mixture is allowed to warm to RT, stirred at RT for 30 min and concentrated in vacuo. The residue is partitioned between water and ether and the aqeuous layer acidified and extracted with ether. The ether extract is washed, dried over Na2SO4, filtered and the filtrate evaporated in vacuo producing a liquid which is crystallized from toluene yielding the desired product as a solid, M.P. 94°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04788187 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-2f308aa42ad447f38a384a06d982668a |
|---|
| Source note | uspto-grants-1988_11 |
|---|