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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057164Generated: November 2, 2026

Sodium Iodide → 3-Chloro-2-fluorobenzyl isothiocyanate

https://huagongshe.com/reaction/2057164

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 numberUS07335803B2
Source datasetuspto-grants-2008_02
ORD IDord-dd9641cd2f7149b18f3611634dd6c57f
Source noteuspto-grants-2008_02