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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751177Generated: October 25, 2026

4-Pentyn-1-ol → 4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]-

https://huagongshe.com/reaction/751177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Pentyn-1-olHCID 79346—
Reactant1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
CatalystHCID 178418397HCID 178418397—
SolventPiperidineHCID 8082—
Product4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]-HCID 6882269083%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1-iodo-4-trifluoromethoxy-benzene (5 g, 17 mmol), Pd(PPh3)4 (973 mg, 1 mmol) and cuprous iodide (160 mg, 1 mmol) in piperidine (130 ml) was stirred for 30 min at 50° C. under an argon atmosphere. 4-Pentyn-1-ol (2.13 g, 25 mmol) was added within 60 min at 50° C. The temperature was raised to 80° C. and the mixture was stirred for 3 h at this temperature. The reaction mixture was cooled to ambient temperature, poured into a solution of saturated aqueous 10% KHSO4/ice water 1/1 and extracted two times with tert butyl methyl ether. The combined extracts were washed with water and brine (two times) and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, heptane/AcOEt) to give 3.4 g (13.9 mmol, 83%) of the title compound as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405236B2
Source datasetuspto-grants-2008_07
ORD IDord-f6ab7523c228421a8da74e83dd1e4169
Source noteuspto-grants-2008_07