Hydrochloric Acid → 7-(Trifluoromethyl)-1H-indole

HRID 550154

反応式

HRID 550154 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][C:9](=O)[C:8]2=O.B(F)(F)F.CCOCC.[BH4-].[Na+].Cl>C1COCC1.O>[F:15][C:2]([F:1])([F:14])[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][CH:9]=[CH:8]2

参加物

7

反応条件

温度
-20 °C

実験手順

To a stirred mixture of 7-trifluoromethyl-1H-indole-2,3-dione (116 mg) in THF (5.00 mL) was added boron trifluoride etherate (0.205 mL, 1.62 mmol) followed by sodium borohydride (71.4 mg, 1.88 mmol). The resulting mixture was stirred at -20° C. for 2 hrs, then water (1 mL) was added and the mixture was stirred at 0° C. for 10 min. The solution was acidified to pH=1 with 2N HCl, warmed to r.t. and stirred at r.t. for 20 min prior to extraction with EtOAc. The extracts were dried over magnesium sulphate, concentrated in vacuo and the residue purified by chromatography over silica gel eluting with hexane to give 7-trifluoromethyl-1H-indole. 1H NMR (400 MHz, CDCl3) δ ppm 6.63-6.68 (1 H, m), 7.20 (1 H, t, J=7.71 Hz), 7.30-7.35 (1 H, m), 7.47 (1 H, d, J=7.33 Hz), 7.83 (1 H, d, J=8.08 Hz), and 8.56 (1 H, br. s.).

後処理

  1. stirringthe mixture was stirred at 0° C. for 10 min
  2. temperaturewarmed to r.t.
  3. stirringstirred at r.t. for 20 min
  4. extractionto extraction with EtOAc
  5. dry with materialThe extracts were dried over magnesium sulphate
  6. concentrationconcentrated in vacuo
  7. customthe residue purified by chromatography over silica gel eluting with hexane

出典と根拠

ORDレコード
ord-ac421b94dde243209ef42c6a1ae42d70
出典データセット
uspto-grants-2011_05
特許番号
US07943767B2

関連ノート

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