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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200052Generated: November 2, 2026

Ethanol → HCID 54225068, compound

https://huagongshe.com/reaction/1200052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant5-[2-(Benzo[b]thiophen-3-yl)ethenyl]thiophene-2-carboxaldehydeHCID 53735268—
SolventWaterHCID 962—
ProductHCID 54225068HCID 5422506871.1%

Reaction Steps

A stirred, chilled (0° C.) suspension of sodium borohydride (0.50 g) and absolute ethanol (250 ml), under nitrogen, was treated in portions with 5-[2-(benzo[b]thiophen-3-yl)ethenyl]thiophene-2-carboxaldehyde (3.0 g). After stirring at room temperature overnight, the mixture was poured into water (250 ml). The organic phase was removed in vacuo, and the resulting aqueous phase was extracted with dichloromethane. The combined, dried over anhydrous magnesium sulfate, filtered organic phase was evaporated. The residue was purified by high performance liquid chromatography (silica gel, loaded and eluted first with dichloromethane, then with ethyl acetate). The appropriate fractions were combined and evaporated. The residue was recrystallized from toluene/hexane to yield 2.15 g (71%) of product, mp 68°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904674
Source datasetuspto-grants-1990_02
ORD IDord-6494c46d63f1486894084b40a77f11cc
Source noteuspto-grants-1990_02