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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244835Generated: November 1, 2026

Triphenylphosphine → 1-(1-Ethynylhexyloxy)-2,3-difluorobenzene

https://huagongshe.com/reaction/2244835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Octyn-3-olHCID 13166—
Reactant2,3-DifluorophenolHCID 80879—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product1-(1-Ethynylhexyloxy)-2,3-difluorobenzeneHCID 59215239—

Reaction Steps

42.4 g (0.33 mol) of 2,3-difluorophenol are initially introduced in 1.2 l of THF together with 50.0 ml (0.34 mol) of 1-octyn-3-ol and 94.1 g (0.36 mol) of triphenylphosphine, and a solution of 76.1 ml (0.39 mol) of DIAD in 100 ml of THF is added dropwise. After 19 h at 20° C., the mixture is diluted with MTBE, and the batch is washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, 1-chlorobutane), giving 1-(1-ethynylhexyloxy)-2,3-difluorobenzene as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678929B2
Source datasetuspto-grants-2010_03
ORD IDord-7ca0ce9827224c2c9edb20222dc523d3
Source noteuspto-grants-2010_03