HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707889Generated: October 27, 2026
2-Methyl-3-butyn-2-ol → 4-(4-Cyanophenyl)-2-methyl-3-butyne-2-ol
https://huagongshe.com/reaction/1707889
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | Benzonitrile, 4-bromo- | HCID 12162 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(4-Cyanophenyl)-2-methyl-3-butyne-2-ol | HCID 2822155 | 79.6% |
Reaction Steps
4-Bromobenzonitrile (30 g), 3-methyl-1-butyne-3-ol (13.4 g), triphenylphosphine (0.7 g) and bis(triphenylphosphine)palladium(II) chloride (0.3 g) were dissolved in triethylamine (140 ml) under nitrogen atmosphere, and then copper(I) iodide (0.1 g) was added thereto. After stirring at room temperature for 1 hour, the reaction mixture was further stirred at 90° C. for 5 hours. The resulting precipitated crystals were filtered, and then triethylamine was distilled off therefrom, followed by extracting with chloroform. The resultant was washed twice with 10% hydrochloric acid, and further with water twice, and then chloroform was distilled off therefrom. The residue was distilled under reduced pressure (140° to 160° C./5 mmHg) to give 3-methyl-1-(4'-cyanophenyl)-1-butyne-3-ol (23.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356558 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-6f64f0fd54944f2c83d704e10dfacb4a |
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| Source note | uspto-grants-1994_10 |
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