HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018659Generated: November 1, 2026
Propargyl alcohol → 3-(4-Chlorophenyl)prop-2-yn-1-ol
https://huagongshe.com/reaction/1018659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(4-Chlorophenyl)prop-2-yn-1-ol | HCID 4111718 | — |
Reaction Steps
A mixture of 6 g of 1-chloro-4-iodo-benzene, 1.8 ml of propargyl alcohol and 5.2 ml of triethylamine in 30 ml of chloroform is placed under a nitrogen atmosphere. 208 mg of bis(triphenylphosphine)palladium(II) dichloride and 98 mg of copper(I) iodide are added thereto. The reaction mixture is stirred for one hour at 40° C. 300 ml of hot n-hexane are then added. The n-hexane phase is decanted off. The residue is again digested with 200 ml of hot n-hexane, and the n-hexane phase is decanted off. The n-hexane phases are concentrated and the residue is subjected to flash chromatography on silica gel with ethyl acetate/n-hexane (1:4), yielding 3-(4-chloro-phenyl)-2-propyn-1-ol, which can be recrystallised from n-hexane, m.p. 78-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482859B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-e77121f440d541d483681898b006e8ff |
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| Source note | uspto-grants-2002_11 |
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