HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546876Generated: October 30, 2026
3-Ethyl-1-pentyn-3-ol → 4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-pentynyl)-3-methyl-phenyl]-propyl}-phenol
https://huagongshe.com/reaction/546876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Ethyl-1-pentyn-3-ol | HCID 22698 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-[1-(4-Bromo-3-methyl-phenyl)-1-ethyl-propyl]-phenol | HCID 57443491 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-pentynyl)-3-methyl-phenyl]-propyl}-phenol | HCID 57443492 | 37% |
Reaction Steps
3-Ethyl-1-pentyn-3-ol (0.754 mL, 5.85 mmol), a [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II), dichloromethane complex (1:1) (482 mg, 0.59 mmol) and copper (I) iodide (112 mg, 0.59 mmol) were added to a solution of 4-[1-(4-bromo-3-methyl-phenyl)-1-ethyl-propyl]-phenol (Example 39-(1); 1.95 g, 5.85 mmol) in triethylamine (10 mL), and the mixture was stirred with microwave heating at 160° C. for three minutes. The reaction mixture was then poured into a saturated aqueous sodium bicarbonate solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=100:0 to 30:70, 40 minutes) to give the target compound as a colorless oil (0.79 g, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935688B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-45375e918a3f49e1b8cdbca7bb0a1b4e |
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| Source note | uspto-grants-2011_05 |
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