HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62783Erstellt: 25. Oktober 2026
Cyclopentanone → 1-(2-(Trifluoromethyl)phenyl)cyclopentanol
https://huagongshe.com/reaction/62783
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyclopentanone | HCID 8452 | — |
| Edukt | Benzene, 1-bromo-2-(trifluoromethyl)- | HCID 9806 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(2-(Trifluoromethyl)phenyl)cyclopentanol | HCID 62802140 | 48,9% |
Reaktionsschritte
A solution of 1-bromo-2-(trifluoromethyl)benzene (0.5 g, 2.222 mmol) in anhydrous THF (10 mL) was cooled to −78° C. (dry ice IPA bath) under argon atmosphere. BuLi (2.5 M in hexanes, 1.068 mL, 2.67 mmol) was added in drops with efficient stirring. The reaction mixture was stirred at −78° C. for 40 min. A solution of cyclopentanone (0.243 g, 2.89 mmol) in anhydrous THF (1.5 mL) was added slowly (in drops) at −78° C. The reaction mixture was stirred at −78° C. for 30 min, gradually brought to room temperature, and stirred for 1 h. The reaction mixture was cooled by an ice bath, quenched with water, and acidified to pH 4-5 by addition of concentrated HCl. The solvent was removed under reduced pressure. The residue was dissolved in methylene chloride, washed with water (2 times), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound as an oil (250 mg). LCMS m/z=213.1 [M−H2O+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447041B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-47fe68485ad74b8da690b0ca7fd0be1b |
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| Quellennotiz | uspto-grants-2016_09 |
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