HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 2-(Trifluoromethyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | (3E)-4-(dimethylamino)-1,1,1-trifluorobut-3-en-2-one | HCID 2063589 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(Trifluoromethyl)quinoline | HCID 2777805 | — |
Reaction Steps
According to instructions in the literature (Baraznenok, I. L., Nenajdenko, V. G., Balenkova, E. S. Eur. J. Org. Chem. 1999, 937–941), 1.2 g (7.18 mmol) of (E)-4-(dimethylamino)-1,1,1-trifluoro-3-buten-2-one is reacted with 2.03 g (7.18 mmol) of trifluoroacetic acid anhydride and 1.30 ml (14.36 mmol) of aniline in 72 ml of 1,2-dichloroethane, then in 36 ml of xylene. After working-up and purification on silica gel with hexane-ethyl acetate (0–100%), 1.01 g (71% of theory) of the product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109212B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-91bcca3662d14d98a4d3c15fbda5f025 |
| Source note | uspto-grants-2006_09 |