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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265413Generated: October 26, 2026

Sodium Iodide → 3-Chloro-2-fluorobenzyl isothiocyanate

https://huagongshe.com/reaction/1265413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-(Bromomethyl)-3-chloro-2-fluorobenzeneHCID 522827—
ReactantIsothiocyanatopotassiumHCID 10931372—
SolventDimethylformamideHCID 6228—
Product3-Chloro-2-fluorobenzyl isothiocyanateHCID 18615680—

Reaction Steps

One molar equivalent of 3-chloro-2-fluoro-benzyl bromide (commercially available from e.g., Lancaster Synthesis, Ltd.) is permitted to react with 2 molar equivalents of potassium isothiocyanate in dimethylformamide (DMF) containing 0.5 molar equivalent of NaI at 90° C. for 5 hours with stirring to yield 3-chloro-2-fluorobenzyl isothiocyanate. The reaction mixture is permitted to cool to room temperature, and the solution is diluted with H2O and extracted with ether. The ether phase containing the product is removed and the reaction mixture extracted twice more with fresh ether. The ether phases are combined and the product is concentrated in a Speed Vac® vacuum centrifuge (using house vacuum) set in a water bath at about 45° C. When the ether has evaporated, the unpurified 3-chloro-2-fluorobenzyl isothiocyanate is a viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545182B2
Source datasetuspto-grants-2003_04
ORD IDord-d7de7c37332940308abffc3421994e4d
Source noteuspto-grants-2003_04