HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylethinylcarbinol → 6-(1-Ethynylbutoxy)-7,8-difluoro-2-pentylchroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylethinylcarbinol | HCID 7746 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 46834772 | HCID 46834772 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(1-Ethynylbutoxy)-7,8-difluoro-2-pentylchroman | HCID 58151900 | — |
Reaction Steps
10.0 g (39.0 mmol) of 7,8-difluoro-2-pentylchroman-6-ol are initially introduced in 140 ml of THF together with 4.0 g (41.0 mmol) of 1-hexyn-3-ol and 11.3 g (42.9 mmol) of triphenylphosphine, and 9.1 ml (46.8 mmol) of DIAD are added over the course of 20 min with ice-cooling. After 18 h at RT, water is added, and the mixture is extracted a number of times with MTBE. The combined organic phases are washed with water and saturated sodium chloride soln., and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-heptane:MTBE=2:1), giving 6-(1-ethynylbutoxy)-7,8-difluoro-2-pentylchroman as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08303844B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-2fd8d632df444939aeb159f484faf82f |
| Source note | uspto-grants-2012_11 |