HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenylhydrazine → 4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenylhydrazine | HCID 12158 | — |
| Reactant | 2-Chloro-6-fluorobenzaldehyde | HCID 67847 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]aniline | HCID 90033658 | 31.4% |
Reaction Steps
To a solution of 2-chloro-6-fluorobenzaldehyde (1.0 g, 6.32 mmol) in ethanol was added (4-bromophenyl)hydrazine (1.7 g, 7.59 mmol) and aq. solution of NaHCO3 (0.637 g, 4.59 mmol). The reaction mixture was stirred at RT for 5-6 h. The reaction mass was quenched in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated. The obtained crude product was purified by column chromatography on silica gel, eluting with 4.6% EA: pet. ether to afford 0.650 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 6.98 (d, J=7.8 Hz, 2H), 7.23-7.40 (m, 5H), 8.07 (s, 1H), 10.87 (br s, 1H). MS (m/z): 329.17 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09439890B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-711f195bc98643a6be7af84972bc0651 |
| Source note | uspto-grants-2016_09 |