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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375628Generated: October 31, 2026

Pyridine → N-hydroxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/1375628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium ChlorideHCID 5234—
Reactant(Z)-Benzaldehyde oximeHCID 12143—
ReactantChlorosuccinimideHCID 31398—
SolventChloroformHCID 6212—
ProductN-hydroxybenzenecarboximidoyl chlorideHCID 275631589%

Reaction Steps

To benzaldehyde oxime (12.2 g, 0.1 mol) in chloroform was added catalytic amount of pyridine, followed by N-chlorosuccinimide (13.35 g, 0.1 mol) at room temperature. The reaction mixture was stirred for 1.5 h, then saturated aqueous NaCl was added. The organic phase was washed with saturated aqueous NaCl (twice) and dried with MgSO4. The solvent was removed under reduced pressure. 13.85 g α-chlorobenzaldehyde oxime was obtained. The yield was 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169798B2
Source datasetuspto-grants-2007_01
ORD IDord-e0e02c3fab8641aa9493a4ffcbcf26b0
Source noteuspto-grants-2007_01