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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt(Trifluoromethyl)trimethylsilaneHCID 552549—
Edukt1-(6-Bromoquinolin-2-yl)ethanoneHCID 57458165—
KatalysatorTetrabutylammonium FluorideHCID 2724141—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(6-Bromoquinolin-2-yl)-1,1,1-trifluoropropan-2-olHCID 57458166105,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08158650B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-28786fdef50f42f7923fb0988b47e921
Quellennotizuspto-grants-2012_04