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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59227Generated: October 27, 2026

2-Chloro-6-fluorobenzaldehyde → N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]-4-iodoaniline

https://huagongshe.com/reaction/59227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-fluorobenzaldehydeHCID 67847—
Reactant4-IodophenylhydrazineHCID 704591—
SolventEthanolHCID 702—
ProductN-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]-4-iodoanilineHCID 9002016675%

Reaction Steps

To a solution of (4-iodophenyl)hydrazine (1.0 g, 4.27 mmol) in ethanol (10 mL) was slowly added solution of 2-chloro-6-fluorobenzaldehyde (0.675 g, 4.27 mmol) in ethanol (10 mL). The reaction mass was stirred at RT for 5-6 h. The reaction mass was quenched in water and extracted with ethyl acetate. The organic layer was concentrated to afford 1.2 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 6.87 (d, J=8.4 Hz, 2H), 7.26-7.36 (m, 3H), 7.53 (d, J=9.0 Hz, 2H), 8.06 (s, 1H), 10.84 (s, 1H). MS (m/z): 374.87 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439890B2
Source datasetuspto-grants-2016_09
ORD IDord-2595c5be4d374fcaa4ba35c003b99004
Source noteuspto-grants-2016_09