HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)aniline → HCID 19978912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19978912 | HCID 19978912 | 104.8% |
Reaction Steps
To a toluene (200 mL) solution of 3-aminobenzotrifluoride (10.4 grams, 0.06 mol) was added 2-fluorobenzaldehyde (8.0 grams, 0.06 mol). The mixture was heated under reflux with a Dean-Stark trap for 6 hours. The solvent was removed in a rotary evaporator to give 2-fluorobenzylidene 3-trifluoromethylaniline (16.8 grams, 97% yield, yellow liquid) whose structure was confirmed by nuclear magnetic resonance, infra-red spectroscopy, and mass spectroscopy analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05076832 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-5570d17b91f744f8b364457c7e45387a |
| Source note | uspto-grants-1991_12 |