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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59223Erstellt: 26. Oktober 2026

4-Bromophenylhydrazine → 4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]aniline

https://huagongshe.com/reaction/59223

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromophenylhydrazineHCID 12158—
Edukt2-Chloro-6-fluorobenzaldehydeHCID 67847—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
Produkt4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]anilineHCID 9003365831,4%

Reaktionsschritte

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)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09439890B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-711f195bc98643a6be7af84972bc0651
Quellennotizuspto-grants-2016_09