Nitroethane → 6-fluoro-3-(2-nitropropenyl)-1H-indole

HRID 37917

反応式

HRID 37917 の反応式
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:11]=O)=[CH:7][NH:8]2)=[CH:4][CH:3]=1.[N+:13]([CH2:16][CH3:17])([O-:15])=[O:14].C([O-])(=O)C.[NH4+]>CCOC(C)=O>[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:11]=[C:16]([N+:13]([O-:15])=[O:14])[CH3:17])=[CH:7][NH:8]2)=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 6587NitroethaneHCID 2629036-Fluoroindole-3-carboxaldehydeHCID 517165Ammonium Acetate

生成物 1

HCID 666405126-fluoro-3-(2-nitropropenyl)-1H-indole収率 86%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared by combining 6-fluoroindole-3-carboxaldehyde (485 mg, 2.97 mmol), nitroethane (6.0 mL), and ammonium acetate (250 mg, 3.27 mmol). The reaction solution was allowed to reflux 2 hours. The reaction solution was diluted with EtOAc (100 mL), washed with H2O (50 mL×2), partitioned, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide 560 mg (86% yield) of 6-fluoro-3-(2-nitropropenyl)-1H-indole; 1H NMR (CDCl3) δ 11.03 (1H, br s), 8.41 (1H, s), 7.63 (1H, dd), 7.50 (1H, s), 7.06 (1H, dd), 6.92 (1H, t), 2.44 (3H, s); TLC (SiO2 plate, 100% DCM) Rf=0.7.

後処理

  1. custom6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared
  2. temperatureto reflux 2 hours
  3. washwashed with H2O (50 mL×2)
  4. custompartitioned
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-a6adde18e4e0446c863bbe24ebf188b1
出典データセット
uspto-grants-2013_09
特許番号
US08524704B2

関連ノート

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