HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Difluorobenzylamine → HCID 22051191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Difluorobenzylamine | HCID 2733244 | — |
| Reactant | HCID 54724162 | HCID 54724162 | — |
| Product | HCID 22051191 | HCID 22051191 | — |
Reaction Steps
The product from Step 2 (0.5 g, 2.28 mmol) and 2,4-difluoro benzylamine (4 mL, 33.6 mmol) were combined in a nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo and the residue was chromatographed on silica (95:5 ethyl acetate:methanol). The final compound was isolated as a light yellow solid (0.16 g, 36%). 1H NMR (400 MHz, CD3OD) δ 7.33 (m, 3H), 7.03 (d, J=8 Hz, 1H), 6.96 (m, 3H), 6.95 (m, 1H), 5.97 (dd, J=3.2 and 8.0 Hz, 1H), 5.48 (d, J=2.56 Hz, 1H), 5.02 (s, 2H), 4.33 (s, 2H) ppm. 19F NMR (400 MHz, CD3OD) δ −113.88 (1F), −115.33 (1F), −116.78 (1F) ppm. ES-HRMS m/z 345.1221 (M+H calcd for C19H17F3N2O requires 345.1209).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07629363B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-35f4a892fe22426a832dd7449f64e591 |
| Source note | uspto-grants-2009_12 |