1,2-Dichloro-4-nitrobenzene → 3,4-Dichloroaniline

HRID 1738617Notes

Reaction equation

HRID 1738617 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N+:9]([O-])=O)[CH:5]=[CH:6][C:7]=1[Cl:8]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[Cl:8])[NH2:9]

Participants

3

Procedure

22.1 g of 3,4-dichloro-nitrobenzene and 70 g of toluene are placed in an agitator autoclave, and the catalyst suspension is flushed in with 4 g of water. Hydrogenation subsequently takes place at a temperature of 100° C. and at a hydrogen pressure of 5 bar. When the hydrogen up-take is complete, the autoclave is cooled and rendered inert with nitrogen. The catalyst is filtered off and washed with toluene. After working up by distillation, 18.0 g of 3,4-dichloroaniline (yield 96.8% of theory) are obtained.

Workup

  1. customthe catalyst suspension is flushed in with 4 g of water
  2. customat a temperature of 100° C.
  3. temperaturethe autoclave is cooled
  4. filtrationThe catalyst is filtered off
  5. washwashed with toluene

Sources & evidence

ORD record
ord-7c1f63ee572a4a1db4be640f97c5e6bb
Source dataset
uspto-grants-1999_10
Patent number
US05962741

Reaction notes

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