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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905733Generated: November 1, 2026

2-Cyano-3-(4-methoxyphenyl)prop-2-enoic acid → 2-Cyano-3-(4-methoxyphenyl)propanoic acid

https://huagongshe.com/reaction/1905733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyano-3-(4-methoxyphenyl)prop-2-enoic acidHCID 233260—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
Product2-Cyano-3-(4-methoxyphenyl)propanoic acidHCID 13711148—

Reaction Conditions

Temperature15 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04647559
Source datasetuspto-grants-1987_03
ORD IDord-80228c2ffa024112afd2c3ffed7585c6
Source noteuspto-grants-1987_03