2-Bromopyridine → 2-[(3-Nitro-2,4-dimethylphenyl)-amino]-pyridine

HRID 981860ノート

反応式

HRID 981860 の反応式
[N+:1]([C:4]1[C:5]([CH3:12])=[C:6]([CH:8]=[CH:9][C:10]=1[CH3:11])[NH2:7])([O-:3])=[O:2].Br[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1.C(=O)([O-])[O-].[Na+].[Na+]>O>[N+:1]([C:4]1[C:5]([CH3:12])=[C:6]([NH:7][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[CH:8]=[CH:9][C:10]=1[CH3:11])([O-:3])=[O:2]

参加物

5

反応物 3

HCID 79732-BromopyridineHCID 10340Sodium CarbonateHCID 133699632,4-Dimethyl-3-nitroaniline

生成物 1

HCID 200683482-[(3-Nitro-2,4-dimethylphenyl)-amino]-pyridine収率 41.4%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
20 °C

実験手順

3.3 g of 3-Nitro-2,4-dimethylaniline and 3.2 g of 2-bromo-pyridine are mixed and the resulting mixture heated for 8 hours to 170° C. After cooling to 20° C., the greasy mass formed was dissolved in water and the solution pH then raised by addition of sodium carbonate. The resulting precipitate was recrystallized from ethanol. 2 g of the product melting at 178° to 179° C. were obtained. Another 2.1 g of the substance were obtained from the aqueous phase by concentration.

後処理

  1. temperaturethe resulting mixture heated for 8 hours to 170° C
  2. customthe greasy mass formed
  3. customThe resulting precipitate was recrystallized from ethanol

出典と根拠

ORDレコード
ord-5333816ef9e6458dacbd323df6c64b6c
出典データセット
uspto-grants-1991_02
特許番号
US04994087

反応ノート

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