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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731541Generated: October 31, 2026

Benzene, 1-chloro-4-ethynyl- → 1-(4-Chlorophenyl)-4,4-dimethyl-5-fluoro-3-(1,2,4-triazol-1-ylmethyl)-1-pentin-3-ol

https://huagongshe.com/reaction/1731541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-chloro-4-ethynyl-HCID 70118—
Reactant4-Fluoro-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-oneHCID 12769539—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chlorophenyl)-4,4-dimethyl-5-fluoro-3-(1,2,4-triazol-1-ylmethyl)-1-pentin-3-olHCID 1334229861.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

62 ml of butyl-lithium (15% strength in hexane, 0.1 mol) are added dropwise to 13.65 g (0.1 mol) of 4-chlorophenyl-acetylene in 50 ml of absolute tetrahydrofuran at 0° C., under nitrogen. The mixture is subsequently stirred at 0° C. for 15 minutes, and 18.5 g (0.1 mol) of 3,3-dimethyl-4-fluoro-1-(1,2,4-triazol-1-yl)-2-butanone in 30 ml of absolute tetrahydrofuran are then added dropwise. Thereafter, the reaction mixture is allowed to warm to room temperature and is subsequently stirred for 14 hours. It is concentrated by distilling off some of the solvent, the residue is taken up in ether and the mixture is washed neutral with water, dried over sodium sulphate and concentrated. The residue is recrystallized from diisopropyl ether. 19.9 g (61.9% of theory) of 1-(4-chlorophenyl)-4,4-dimethyl-5-fluoro-3-(1,2,4-triazol-1-ylmethyl)-1-pentin-3-ol or melting point 120° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622333
Source datasetuspto-grants-1986_11
ORD IDord-a18548789fd948748abba5ef07517f1e
Source noteuspto-grants-1986_11