HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorobenzhydrazide → HCID 178427628, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorobenzhydrazide | HCID 136288 | — |
| Reactant | HCID 18406860 | HCID 18406860 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178427628 | HCID 178427628 | — |
Reaction Steps
The product from step c) (10 g, 0.028 mol) was suspended in xylene (250 ml) with 2-fluorobenzoic hydrazide (4.7 g, 0.0231 mol) and heated under reflux for 3 h. After cooling, the reaction mixture was filtered and the solid produced was washed in the sinter funnel several times with dichloromethane then concentrated under vacuum to leave a solid (10.53 g). The product existed as a 1:1 mixture of 2 tautomers. 1H NMR (400 MHz, CDCl3) δ 2.37 (3H, s), 7.18-7.66 (12H, m), 8.06 (1H, s), 11.90 (0.5H, s), 13.78 (0.5H, s); MS (ES+) m/e 497 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476030B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-63936a510eb44100bf3004bf3564773b |
| Source note | uspto-grants-2002_11 |