HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Anilino-7-trifluoromethylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Chloro-7-(trifluoromethyl)quinazoline | HCID 12806742 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Anilino-7-trifluoromethylquinazoline | HCID 12806773 | 60% |
Reaction Steps
2.5 g of 4-chloro-7-trifluoromethylquinazoline were dissolved in 10 ml of ethanol, and 1.0 g of aniline was added to the solution. Reaction occurred violently and the reaction mixture solidified immediately. After cooling, the solidified product was collected and washed with ethanol. The resulting crystals were pulverized and added to a dilute aqueous solution of sodium hydroxide. Insolubles were filtered off and recrystallized from ethanol to give 1.7 g (yield 60%) of the desired Compound No. 17 in the form of colourless plates melting at 230°-232° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464375 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-286f2e10af6c4eb48b67a76a2bfad034 |
| Source note | uspto-grants-1984_08 |