HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1693072Erstellt: 26. Oktober 2026
Hydrochloric Acid → 2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-ol
https://huagongshe.com/reaction/1693072
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Edukt | 1-(6-Bromoquinolin-2-yl)ethanone | HCID 57458165 | — |
| Katalysator | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-ol | HCID 57458166 | 105,1% |
Reaktionsschritte
A DMF (5 ml) solution of 1-(6-bromoquinolin-2-yl)ethanone (129 mg, 0.52 mmol), (trifluoromethyl)trimethylsilane (220 mg, 1.55 mmol) and tetrabutylammonium fluoride (13.5 mg, 0.052 mmol) was stirred at 100° C. for 2 hours. Then the mixture was cooled to room temperature and 1N-hydrochloride aqueous solution (2 ml) was added. After 4 hours, the mixture was quenched with saturated sodium bicarbonate aqueous solution, and the product was extracted with ethyl acetate which was dried over sodium sulfate. Then, filtration, evaporation and purification through silica gel column chromatography, eluting with hexane/ethyl acetate (4:1), furnished the title compound (175 mg, quant.) as a white solid. 1H NMR (300 MHz, CDCl3) δ 1.81 (3H, s), 6.51 (1H, s), 7.64 (1H, d, J=8.1 Hz), 7.66-7.89 (1H, m), 8.00-8.12 (2H, m), 8.21 (1H, d, J=8.8 Hz). MS (ESI): m/z 320, 322 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08158650B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-28786fdef50f42f7923fb0988b47e921 |
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| Quellennotiz | uspto-grants-2012_04 |
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