Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873308Generated: November 4, 2026

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

https://huagongshe.com/reaction/1873308

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

2.4 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 RT, the batch is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with saturated sodium chloride solution. The solution is dried using sodium sulfate and evaporated 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 numberUS08303844B2
Source datasetuspto-grants-2012_11
ORD IDord-99a9c6d81ce54503a22202bff0fb1439
Source noteuspto-grants-2012_11