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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980794Generated: October 31, 2026

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

https://huagongshe.com/reaction/980794

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 aqueous 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 numberUS04639442
Source datasetuspto-grants-1987_01
ORD IDord-2ebf1a6f27a740fdad2214f3df4107a4
Source noteuspto-grants-1987_01