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HRID 1791420作成日:2026年10月26日

Sodium Carbonate → 1-[4-(tert-butyl)benzyl]-6-[4-(trifluoromethyl)phenyl]-1H-indole

https://huagongshe.com/reaction/1791420

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
反応物6-bromo-1-[4-(tert-butyl)benzyl]-1H-indoleHCID 22032927—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1-[4-(tert-butyl)benzyl]-6-[4-(trifluoromethyl)phenyl]-1H-indoleHCID 2203294867.3%

反応手順

Following the procedure described in Step 2 of Example 5, 6-bromo-1-[4-(tert-butyl)benzyl]-1H-indole (0.490 g, 1.43 mmol) was coupled to 4-trifluoromethylbenzeneboronic acid (0.300 g, 1.58 mmol), using tetrakis(triphenylphosphine)palladium (0.0560 g, 0.0484 mmol) and sodium carbonate (0.615 g, 5.80 mmol) in water (2.8 mL), ethanol (1.4 mL) and toluene (10 mL). Purification by flash chromatography using hexane as an eluant afforded 1-[4-(tert-butyl)benzyl]-6-[4-(trifluoromethyl)phenyl]-1-H-indole as a white solid (0.392 g, 67%), mp 134-135° C. 1HNMR (200 MHz, DMSO-d6): δ 7.85 (d, 3H, J=7.7 Hz), 7.75 (d, 2H, J=7.7 Hz), 7.65 (d, 1H, J=7.7 Hz), 7.55 (d, 1H, J=4.1 Hz), 7.25-7.4 (m, 3H), 7.15 (d, 2H, J=7.7 Hz), 6.5 (d, 1H, J=2.6 Hz), 5.45 (s, 2H), and 1.2 ppm (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07074817B2
出典データセットuspto-grants-2006_07
ORD IDord-a864c9c08e5647ed97b84d93553ff09c
出典メモuspto-grants-2006_07