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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646721Generated: October 25, 2026

Dichloromethane → 2-fluoro-N-hydroxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/1646721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzaldehyde, 2-fluoro-, oximeHCID 587025—
Product2-fluoro-N-hydroxybenzenecarboximidoyl chlorideHCID 3758118—

Reaction Conditions

Temperature-10 °C

Reaction Steps

In 1 liter dichloromethane was dissolved 55.0 g 2-fluorobenzaldehyde oxime at room temperature with stirring. The resulting solution was cooled to -10° C. and Cl2 was bubbled in at such a rate to maintain the temperature below 15° C. After a dark blue color was generated (2-3 minutes) a solution of triethylamine (50 ml) in dichloromethane (100 ml) was added dropwise concurrently with Cl2 addition. When the reaction mixture had maintained a yellow color, additions of the triethylamine solution and Cl2 were discontinued. Concentration of the reaction mixture left an oil which was dissolved in ether and washed four times with 3N HCl followed by a final wash with brine. The organic layer was dried (MgSO4), filtered and concentrated in vacuo to give 60.0 g of 2-fluoro-N-hydroxybenzenecarboximidoyl chloride as an oil which solidified on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180834
Source datasetuspto-grants-1993_01
ORD IDord-14f8df8d2e4449068d253e65c2d8bf23
Source noteuspto-grants-1993_01