Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120851Generated: November 2, 2026

Pyridine → N-hydroxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/2120851

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 numberUS06693108B2
Source datasetuspto-grants-2004_02
ORD IDord-b7940cd39b45435c9b2d625235ac7f5f
Source noteuspto-grants-2004_02