HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 751177Erstellt: 25. Oktober 2026
4-Pentyn-1-ol → 4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]-
https://huagongshe.com/reaction/751177
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Pentyn-1-ol | HCID 79346 | — |
| Edukt | 1-Iodo-4-(trifluoromethoxy)benzene | HCID 2777294 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Piperidine | HCID 8082 | — |
| Produkt | 4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]- | HCID 68822690 | 83% |
Reaktionsschritte
A mixture of 1-iodo-4-trifluoromethoxy-benzene (5 g, 17 mmol), Pd(PPh3)4 (973 mg, 1 mmol) and cuprous iodide (160 mg, 1 mmol) in piperidine (130 ml) was stirred for 30 min at 50° C. under an argon atmosphere. 4-Pentyn-1-ol (2.13 g, 25 mmol) was added within 60 min at 50° C. The temperature was raised to 80° C. and the mixture was stirred for 3 h at this temperature. The reaction mixture was cooled to ambient temperature, poured into a solution of saturated aqueous 10% KHSO4/ice water 1/1 and extracted two times with tert butyl methyl ether. The combined extracts were washed with water and brine (two times) and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, heptane/AcOEt) to give 3.4 g (13.9 mmol, 83%) of the title compound as orange oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07405236B2 |
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| Quelldatensatz | uspto-grants-2008_07 |
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| ORD ID | ord-f6ab7523c228421a8da74e83dd1e4169 |
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| Quellennotiz | uspto-grants-2008_07 |
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