1,2-Dichloro-4-nitrobenzene → 3,4-Dichloroaniline
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
Reactant 1
Product 1
Reagents, catalysts & solvents 1
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
- customthe catalyst suspension is flushed in with 4 g of water
- customat a temperature of 100° C.
- temperaturethe autoclave is cooled
- filtrationThe catalyst is filtered off
- washwashed with toluene
Sources & evidence
- ORD record
- ord-7c1f63ee572a4a1db4be640f97c5e6bb
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05962741
Reaction notes
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