HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764999Generated: October 27, 2026
Propylethinylcarbinol → HCID 23115712, compound
https://huagongshe.com/reaction/1764999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylethinylcarbinol | HCID 7746 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1,2,3-Trifluoro-4-iodobenzene | HCID 2779253 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Copper iodide | HCID 83717 | — |
| Product | HCID 23115712 | HCID 23115712 | — |
Reaction Steps
In a nitrogen atmosphere, 4-iodo-1,2,3-trifluorobenzene was dissolved into DMF, into which triethylamine, copper iodide (I), and tetrakistriphenylphosphine palladium (0) were added and heated to 55° C. Then, the DMF solution containing 1-hexine-3-ol was added dropwise for 20 minutes, and stirred for 3 hours. After the reaction mixture was poured into a sodium thiosulfate aqueous solution, and stirred for a while, an organic layer was separated, and an aqueous layer was extracted with toluene. After the extract and the organic layer were mixed together, washed using water, 10% hydrochloric acid twice, water, a saturated sodium hydrogen carbonate aqueous solution, and a saturated saline solution in that order, and dried using anhydrous magnesium sulfate, the solvent was evaporated under a reduced pressure. The residue was purified by column chromatography (silica gel, toluene/hexane) to obtain 1-(3-hydroxy-1-hexynyl)-2,3,4-trifluorobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07226644B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-2ea8aa046b1043538a0c3827bc9bb26d |
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| Source note | uspto-grants-2007_06 |
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