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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105879Generated: October 25, 2026

Sodium Iodide → 2-Benzyl-5-(N,N-dimethylthiocarbamoyl)thio-4-isothiazolin-3-one

https://huagongshe.com/reaction/1105879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-benzyl-5-chloroisothiazol-3(2H)-oneHCID 4345152—
ReactantSodium dimethyldithiocarbamate dihydrateHCID 23693613—
SolventEthanolHCID 702—
Product2-Benzyl-5-(N,N-dimethylthiocarbamoyl)thio-4-isothiazolin-3-oneHCID 1285272760%

Reaction Steps

To a solution of 6.76 g. (0.03 mole) of 2-benzyl-5-chloro-4-isothiazolin-3-one in 25 ml of ethanol was added a solution of 5.37 g. (0.03 mole) of N,N-dimethyldithiocarbamic acid sodium salt dihydrate in 30 ml of ethanol followed by 0.1 g. of sodium iodide. A yellow solid separated spontaneously. The mixture was stirred at room temperature for 3 hours, then cooled and filtered. The solid was triturated with 50 ml of water and recrystallized from 250 ml of boiling EtOH to give 5.6 g. (60% yield) of the named product, mp 184°-186°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310590
Source datasetuspto-grants-1982_01
ORD IDord-7418178551d446d4aeac9a32f44bb6f8
Source noteuspto-grants-1982_01