HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)aniline → HCID 21110147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Allyl acetoacetate | HCID 70701 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21110147 | HCID 21110147 | — |
Reaction Steps
To a solution of 4-formylbenzonitrile (10.00 g, 76.3 mmol), allyl 3-oxobutanoate (10.84 g, 76.3 mmol), 2,2-dimethyl-1,3-dioxane-4,6-dione (10.99 g, 76.3 mmol) and 3-(trifluoromethyl)aniline (12.29 g, 76.3 mmol) in 150 ml THF are added 4.00 g potassium fluoride on alumina (40 wt.-%). The reaction mixture is stirred at reflux temperature overnight. The solvent is removed in vacuo, the residue is dissolved in methylene chloride and then purified by column chromatography using a methylene chloride/ethyl acetate gradient as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230017B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-e4346b62e26240468aa6c8f972f14679 |
| Source note | uspto-grants-2007_06 |