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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534721Generated: October 30, 2026

4-Fluorobenzyl chloride → HCID 19907879, compound

https://huagongshe.com/reaction/1534721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl chlorideHCID 9602—
Reactant2,3-DiaminopyridineHCID 9956—
ReactantAmmonium HydroxideHCID 14923—
SolventChloroformHCID 6212—
ProductHCID 19907879HCID 19907879—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3 parts of 2,3-pyridinediamine and 4 parts of 1-(chloromethyl)-4-fluorobenzene was stirred overnight at 120° C. Trichloromethane and a dilute ammonium hydroxide solution were added and the product was extracted. The organic phase was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The second fraction was collected and the eluent was evaporated, yielding 1.8 parts of N3 -[(4-fluorophenyl)methyl]-2,3-pyridinediamine as a residue (intermediate 18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE033833
Source datasetuspto-grants-1992_02
ORD IDord-f6f6122aada1421cb0ac38b963acb7ba
Source noteuspto-grants-1992_02