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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651790Generated: November 2, 2026

4-Hydroxybenzaldehyde → HCID 23050521, compound

https://huagongshe.com/reaction/1651790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Propyne, 3-(1-ethoxyethoxy)-HCID 86774—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23050521HCID 23050521—

Reaction Steps

A solution of 16 g (124.8 mmol) of 1-(1-ethoxyethoxy)-2-propyne in 270 ml of tetrahydrofuran was treated at -78° under argon with 78 ml of n-butyllithium (1.6 M in hexane). The mixture was stirred at -40° for 30 minutes and then a solution 7.62 g (62.4 mmol) of 4-hydroxybenzaldehyde 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)-(4-hydroxyphenyl)-2-butyn-1-ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929741
Source datasetuspto-grants-1990_05
ORD IDord-5fb2dee539de4ff1ab38e274bd3ffb71
Source noteuspto-grants-1990_05