Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651784Generated: November 2, 2026

4-Methylbenzaldehyde → HCID 23050505, compound

https://huagongshe.com/reaction/1651784

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Propyne, 3-(1-ethoxyethoxy)-HCID 86774—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23050505HCID 23050505—

Reaction Steps

A solution of 5 g (33 mmol) of 1-(1-ethoxyethoxy)-2-propyne in 84 ml of tetrahydrofuran was treated at -78° under argon with 24.4 ml of n-butyllithium (1.6M in hexane). The mixture was stirred at -40° for 30 minutes and then a solution of 4.6 ml (33 mmol) of 4-methylbenzaldehyde in 34 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 60 ml of saturated ammonium chloride solution. The aqueous phase was extracted twice with ether. 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 chromatography on 500 g of silica gel (elution agent ether/hexane 1:1). There was obtained 4-(1-ethoxyethoxy)-1-(4-methylphenyl)-2 -butyn-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929741
Source datasetuspto-grants-1990_05
ORD IDord-85886e1290a14bd0a9eda1a8870a7ace
Source noteuspto-grants-1990_05