HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)aniline → HCID 20512459, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | Alpha,alpha,alpha-trifluoro-M-toluidine hydrochloride | HCID 200755 | — |
| Reactant | HCID 13674776 | HCID 13674776 | — |
| Reactant | HCID 70530311 | HCID 70530311 | — |
| Product | HCID 20512459 | HCID 20512459 | 42.4% |
Reaction Steps
1-(2',6'-Dimethylphenyl-amino)-2-(3'-trifluoromethylphenyl-amino)-propane, applied as starting substance, is prepared by reacting N-(β-chloropropyl)-2,6-dimethyl-aniline, a compound prepared as described in Example 3, Method (b), point (a), with 3-trifluoromethyl-aniline. The reaction is performed as described in Example 16, point (c) with the difference that crystalline 3-trifluoromethyl-aniline hydrochloride is separated from the reaction mixture by trituration with benzene. The aimed product is obtained with a yield of 42.4%; m.p.: 160°-166° C. (dihydrochloride).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284642 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-b7201b92b3d0407c967ad34ba7d65a0c |
| Source note | uspto-grants-1981_08 |