HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 1-(2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzylidene)-2-methylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzaldehyde | HCID 86638472 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzylidene)-2-methylhydrazine | HCID 66767140 | 76.7% |
Reaction Steps
2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzaldehyde (13.0 g, 31.0 mmol) is refluxed with methylhydrazine (4.3 g, 93 mmol) in THF (130 mL) for 2 hours. The reaction is quenched with water (150 mL) and extracted with MTBE (2×150 mL). The organic layer is washed with saturated sodium chloride aqueous solution (2×150 mL), dried with anhydrous sodium sulfate, and concentrated to obtain a solid. The crude solid is recrystallized in EtOAc/hexane to obtain 1-(2,4-dibromo-5-(2-fluoro-4-nitrophenoxy)benzylidene)-2-methylhydrazine as a yellow solid (10.6 g, 76.7% yield). MS (m/z): 447.9 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE043878E1 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-08f36f1c98aa4dd29b4e989adf9c47eb |
| Source note | uspto-grants-2012_12 |