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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651785Generated: November 1, 2026

Ammonium Chloride → HCID 23050514, compound

https://huagongshe.com/reaction/1651785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant1-Propyne, 3-(1-ethoxyethoxy)-HCID 86774—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23050514HCID 23050514—

Reaction Steps

A solution of 8 g (62.4 mmol) of 1 (1-ethoxyethoxy)-2-propyne in 134 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 6.6 ml (62 mmol) of 4-fluorobenzaldehyde in 54 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 chromatography on 600 g of silica gel (elution agent ether/hexane 1:1). There was obtained 4-(1-ethoxyethoxy)-1-(4-fluorophenyl)-2-butyn- 1-ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929741
Source datasetuspto-grants-1990_05
ORD IDord-5605d4c22b6247859ad721b686ae24af
Source noteuspto-grants-1990_05