HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(1-Ethynylhexyloxy)-2,3-difluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Octyn-3-ol | HCID 13166 | — |
| Reactant | 2,3-Difluorophenol | HCID 80879 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-(1-Ethynylhexyloxy)-2,3-difluorobenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678929B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-7ca0ce9827224c2c9edb20222dc523d3 |
| Source note | uspto-grants-2010_03 |