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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59223Generated: October 26, 2026

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

https://huagongshe.com/reaction/59223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenylhydrazineHCID 12158—
Reactant2-Chloro-6-fluorobenzaldehydeHCID 67847—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]anilineHCID 9003365831.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439890B2
Source datasetuspto-grants-2016_09
ORD IDord-711f195bc98643a6be7af84972bc0651
Source noteuspto-grants-2016_09