HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → N-(3-chloropropyl)-2-nitro-4-(trifluoromethyl)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Propanol, 3-[[2-nitro-4-(trifluoromethyl)phenyl]amino]- | HCID 2847509 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(3-chloropropyl)-2-nitro-4-(trifluoromethyl)benzenamine | HCID 20506352 | — |
Reaction Steps
To a stirred mixture of 26 parts of 3-{[2-nitro-4-(trifluoromethyl)phenyl]amino}-1-propanol and 150 parts of trichloromethane are added dropwise 40 parts of sulfinyl chloride. Upon completion, stirring is continued overnight at reflux temperature. The reaction mixture is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5) as eluent. The pure fractions are collected and the eluent is evaporated, yielding N-(3-chloropropyl)-2-nitro-4-(trifluoromethyl)benzenamine as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250176 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-8a7f95ea7473402a9790d4fa7dcb0096 |
| Source note | uspto-grants-1981_02 |