HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4,5-dichloro-N-(3-chloropropyl) 2-nitrobenzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-((4,5-Dichloro-2-nitrophenyl)amino)-1-propanol | HCID 112955 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4,5-dichloro-N-(3-chloropropyl) 2-nitrobenzenamine | HCID 13105626 | — |
Reaction Steps
To a stirred mixture of 10 parts of 3-[(4,5-dichloro-2-nitrophenyl)amino]-1-propanol and 75 parts of trichloromethane are added dropwise 11.2 parts of sulfinyl chloride. Upon completion, stirring is continued for 4 hours at reflux temperature. The reaction mixture is evaporated and the residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 4,5-dichloro-N-(3-chloropropyl)-2-nitrobenzenamine; mp 78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250176 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-30e96cd76ed84af0a0b29180e3cf6709 |
| Source note | uspto-grants-1981_02 |