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Hydrochloric Acid → HCID 23323482、化合物

HRID 1381129
ノート
印刷プレビュー

反応式

HRID 1381129 の反応式
[H-].[Na+].[NH2:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[C:6]#[N:7].[F:12][C:13]1[CH:14]=[C:15]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:17][CH:18]=1.Cl>CN(C)C=O.O>[F:12][C:13]1[CH:14]=[C:15]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:17][C:18]=1[NH:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[C:6]#[N:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 98231-Fluoro-3-nitrobenzeneHCID 24758Sodium hydrideHCID 729132-Aminobenzonitrile

生成物 1

HCID 23323482HCID 23323482、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228
Dimethylformamide
溶媒

反応条件

温度
80 °C

実験手順

21.8 g (0.5 mol) of sodium hydride were added in portions to a solution of 59 g (0.5 mol) of 2-aminobenzonitrile and 53.2 ml (0.5 mol) of 3-fluoronitrobenzene in absolute dimethylformamide, whereby the reaction mixture warmed up to 80° C., with a change in colour from dark green to dark red. After the mixture had been cooled to room temperature, it was diluted with water and acidified with 2N hydrochloric acid, and the precipitate formed was filtered off. The precipitate was purified by chromatography over silica gel using dichloromethane, and the residue from evaporation of the product-containing fractions was thoroughly stirred with ether/petroleum ether 1:2.

後処理

  1. temperatureAfter the mixture had been cooled to room temperature
  2. customthe precipitate formed
  3. filtrationwas filtered off
  4. customThe precipitate was purified by chromatography over silica gel
  5. customthe residue from evaporation of the product-containing fractions

出典と根拠

ORDレコード
ord-5eeb6bafb555451d9d3d65e3d60c6f9a
出典データセット
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04585772

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート