2-Chloro-5-bromoaniline → (5-Bromo-2-chlorophenyl)hydrazine hydrochloride

HRID 70236ノート

反応式

HRID 70236 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:9])=[C:6]([CH:8]=1)[NH2:7].[N:10]([O-])=O.[Na+]>Cl.O>[ClH:9].[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:9])=[C:6]([NH:7][NH2:10])[CH:8]=1

参加物

5

反応条件

温度
5 °C

実験手順

A suspension of 5-bromo-2-chloroaniline (23 g, 0.11 mol) in concentrated hydrochloric acid (150 mL) and water (90 mL) was cooled in an ice/salt bath. A solution of sodium nitrite (8 g, 0.11 mol) in water (50 mL) was added dropwise to the reaction mixture while maintaining the temperature below 4° C. After stirring for 30 minutes the suspension was transferred via cannula to a solution of SnCl2 dihydrate in concentrated hydrochloric acid (170 mL) and cooled to 5° C. The resulting thick suspension was stirred for 2 h at 5° C. and the solid was isolated via filtration. The solid was air dried and then further dried by adding chlorobutane (500 mL) and refluxing using a Dean-Stark condenser. After cooling, the solid was isolated by filtration to afford the title compound as an off-white solid (35.3 g).

後処理

  1. temperaturewas cooled in an ice/salt bath
  2. temperaturewhile maintaining the temperature below 4° C
  3. stirringThe resulting thick suspension was stirred for 2 h at 5° C.
  4. customthe solid was isolated via filtration
  5. customdried
  6. customfurther dried
  7. additionby adding chlorobutane (500 mL)
  8. temperaturerefluxing
  9. temperatureAfter cooling
  10. customthe solid was isolated by filtration

出典と根拠

ORDレコード
ord-caa1a57369bf467da206bf747fd6b458
出典データセット
uspto-grants-2014_09
特許番号
US08822521B2

反応ノート

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