HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464595Generated: October 31, 2026
Propargyl alcohol → 3-(4-methoxyphenyl)prop-2-yn-1-ol
https://huagongshe.com/reaction/1464595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 4-Iodoanisole | HCID 69676 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-methoxyphenyl)prop-2-yn-1-ol | HCID 12003191 | 94.8% |
Reaction Steps
Diethylamine (80 mL, propargyl alcohol (6.4 mL, 0.11 mol), copper(I)iodide (0.7 g), tetrahydrofuran (25 mL), and tetrakis(triphenylphosphine)palladium(o) (1.2 g) were placed in a 250-mL flask under nitrogen. A solution of p-iodoanisole (23.4 g, 0.1 mol) in 40 mL of tetrahydrofuran was added to the reaction dropwise over 30 minutes. The reaction was stirred for 16 hours at room temperature, then evaporated in vacuo to give a dark brown residue. The residue was dissolved in 200 mL of water and extracted four times with diethyl ether (200 mL). The combined extracts were dried over anhydrous sodium sulfate and evaporated to give a dark brown solid that was purified by column chromatography (silica gel), eluting with 9:1 hexane-ethyl acetate to give 15.38 g of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306718 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-effc7818d44b4bbfaa39cb844d6e89c4 |
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| Source note | uspto-grants-1994_04 |
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