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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34470Generated: October 26, 2026

Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate

https://huagongshe.com/reaction/34470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBromocresol GreenHCID 6451—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoateHCID 54507081—
SolventEthanolHCID 702—
ProductEthyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoateHCID 20129780—

Reaction Steps

A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acetic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761475
Source datasetuspto-grants-1988_08
ORD IDord-62b182c93158406b8248468834a06f6a
Source noteuspto-grants-1988_08