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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911654Generated: November 2, 2026

Chlorosuccinimide → 4-Chloro-N-hydroxybenzimidoyl chloride

https://huagongshe.com/reaction/1911654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant(NZ)-N-[(4-chlorophenyl)methylidene]hydroxylamine;4-fluorobenzaldehydeHCID 87630081—
SolventDimethylformamideHCID 6228—
Product4-Chloro-N-hydroxybenzimidoyl chlorideHCID 727186586.4%

Reaction Steps

To a solution of (E)- and/or (Z)-4-chloro-benzaldehyde oxime 4-fluorobenzaldehyde (27.0 g, 173 mmol) in DMF (173 mL) was added N-chlorosuccinimide (22.8 g, 173 mmol) portionwise over 1 h, keeping the temperature below 35° C. The reaction mixture was stirred at room temperature for 1 h. The mixture was then poured onto ice-water, and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulfate and evaporated to afford the title compound (28.4 g, 86%) which was obtained as a light yellow solid. MS: m/e=189.1 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604062B2
Source datasetuspto-grants-2013_12
ORD IDord-89e21046a7b846fd8e5313bbbe87caa2
Source noteuspto-grants-2013_12