HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873317Generated: November 2, 2026
Propylethinylcarbinol → HCID 58151944, compound
https://huagongshe.com/reaction/1873317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylethinylcarbinol | HCID 7746 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 58151935 | HCID 58151935 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58151944 | HCID 58151944 | — |
Reaction Steps
7.0 g (22.7 mmol) of 3,4-difluoro-6-(4-propylcyclohexyl)-5,6,7,8-tetrahydronaphthalen-2-ol are initially introduced in 90 ml of THF together with 2.70 ml (24.0 mmol) of 1-hexyn-3-ol and 6.60 g (25.2 mmol) of triphenylphosphine. 5.3 ml (46.8 mmol) of DIAD in 10 ml of THF are added over the course of 20 min with ice-cooling. After 19 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-(4-propylcyclohexyl)-1,2,3,4-tetrahydronaphthalene as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08303844B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-95d931fc16054e5aac801142223e3b46 |
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| Source note | uspto-grants-2012_11 |
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