HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Fluoro-2-(trifluoromethyl)phenyl)methanamine → HCID 17819328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Fluoro-2-(trifluoromethyl)phenyl)methanamine | HCID 2734878 | — |
| Reactant | 3-(Tert-butylamino)-4-ethoxycyclobut-3-ene-1,2-dione | HCID 19082433 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 17819328 | HCID 17819328 | 52% |
Reaction Steps
To a room temperature solution of (0.7 g, 3.55 mmol) of 3-ethoxy-4-(tert-butylamino)-cyclobut-3-ene-1,2-dione and THF (30 mL) was added (0.73 g, 3.78 mmol) of the 4-fluoro-2-trifluoromethylbenzylamine via a syringe. The resulting mixture was stirred at room temperature for 12 hours. After concentration in vacuo, the resulting white solid was recrystallized from hot acetonitrile to give 0.55 gm (52%) of 3-tert-butylamino-4-(4-fluoro-2-trifluoromethyl-benzylamino)-cyclobut-3-ene-1,2-dione as a white solid: mp 192°-194° C.; 1H NMR (DMSO-d6) δ1.36 (s, 9H), 4.88 (d, 2H) 7.67 (m, 5H) ppm; IR (KBr) 3250, 2900, 1800, 1580, 1530 cm-1 ; MS (m/z) 345 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780505 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-81d9cbdc76fa4e61997b020c00a123d0 |
| Source note | uspto-grants-1998_07 |