HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)aniline → 3,5-Di(benzyloxy)-3'-(trifluoromethyl)benzanilid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | 3,5-Bis(benzyloxy)benzoyl chloride | HCID 10831869 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Di(benzyloxy)-3'-(trifluoromethyl)benzanilid | HCID 10277296 | — |
Reaction Steps
(Examplary Compound 8). The title compound was prepared according to the procedure of Scheme I-A, starting from 3,5-bis(benzyloxy)benzoic acid chloride and 3-(trifluoromethyl)aniline in THF solution. White solid, yield 0.250 g (69%). 1H NMR (DMSO-d6, 400 MHz), δ: 10.47 (s, 1H); 8.24 (s, 1H); 8.06 (d, J=8.3 Hz, 1H); 7.60 (t, J=8.0 Hz, 1H); 7.51-7.32 (m, 11H); 7.25 (s, 2H); 6.95 (s, 1H); 5.18 (s, 4H). Anal: Calcd. for C28H22F3NO3: 70.43; H, 4.64; N, 2.93. Found: C, 70.58; H, 4.67; N, 2.91.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06656971B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-bbea766bfac34e7cb3a7c065633ef599 |
| Source note | uspto-grants-2003_12 |