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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757273Generated: November 2, 2026

Water → HCID 19390157, compound

https://huagongshe.com/reaction/1757273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-(Thiophen-3-yl)benzaldehydeHCID 4547526—
Reactant(4-Cyanobutyl)(triphenyl)phosphanium bromideHCID 11418829—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 19390157HCID 1939015795.8%

Reaction Steps

44.6 g of 4-cyanobutyl(triphenyl)phosphonium bromide is suspended in 250 ml of dimethylformamide, 4.2 g of 60% oily sodium hydride is added under ice cooling and stirring, the mixture is stirred at that temperature for 30 minutes, 18 g of 3-(3-thienyl)benzaldehyde is added, and the mixture is stirred at room temperature for 20 hours. Water and acetic acid are added to the reaction solution for neutralization, the solvent is distilled off under reduced pressure, and the residue is post-treated in a conventional manner and purified by silica gel column chromatography [Wako gel C-100, 500 g; hexane/ethyl acetate=5/1] to obtain 23.2 g of (E)-3-[3-(5-cyano-1-pentenyl)phenyl]thiophene as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444084
Source datasetuspto-grants-1995_08
ORD IDord-957ecab288764102a76686b5d4bdb67c
Source noteuspto-grants-1995_08