HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dichloronitrobenzene → 4-Chloro-N-[(4-chlorophenyl)methyl]-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-N-[(4-chlorophenyl)methyl]-2-nitroaniline | HCID 14952977 | 57.6% |
Reaction Steps
25 g of 2,5-dichloronitrobenzene and 36.9 g of 4-chlorobenzylamine are heated for two hours at 135° C., it being necessary for the temperature always to be kept below 140° C. After cooling, the mixture is taken up with water and extracted with ethyl acetate. After drying over magnesium sulfate and evaporation under vacuum, the residue is taken up with ether and the crystals obtained are filtered off and washed with ether to give 22.3 g of 2-(4-chlorophenylmethylamino)-5-chloronitrobenzene in the form of crystals melting at 120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05124336 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-5ab13f76a8a94b68abb4500fd2be9b32 |
| Source note | uspto-grants-1992_06 |