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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651792Generated: November 2, 2026

Ammonium Chloride → HCID 23050444, compound

https://huagongshe.com/reaction/1651792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Methylthio)benzaldehydeHCID 76985—
Reactant1-Propyne, 3-(1-ethoxyethoxy)-HCID 86774—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23050444HCID 23050444—

Reaction Steps

A solution of 8 g (62.4 mmol) of 1-(1-ethoxyethoxy)-2-propyne in 135 ml of tetrahydrofuran was treated at -78° under argon with 39 ml of n-butyllithium (1.6M in hexane). The mixture was stirred at -40° for 30 minutes and then a solution of 8.11 ml (62.4 mmol) of 4-(methylthio)benzaldehyde in 53 ml of tetrahydrofuran was added within 10 minutes. The reaction mixture was warmed to 0°, stirred at 0° for a further 1 hour and then treated with 100 ml of saturated ammonium chloride solution. The aqueous phase was extracted twice with ethyl acetate. The combined organic phases were washed in succession with saturated sodium chloride solution and with water, dried over magnesium sulphate and concentrated. The residue was purified by flash chromatography on 600 g of silica gel (elution agent ether/hexane 1:1). There was obtained 4-(1-ethoxyethoxy)-1- [4-(methylthio)phenyl]-2 -butyn-1 ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929741
Source datasetuspto-grants-1990_05
ORD IDord-a25655fa512e4fdd9505c010e9f1d040
Source noteuspto-grants-1990_05