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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415057Generated: October 27, 2026

Methyl iodide → 2-(2-Isopropylphenyl)imino-3-(methylthio)thiocarbonyl-1,3-thiazolidine

https://huagongshe.com/reaction/2415057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178438962HCID 178438962—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(2-Isopropylphenyl)imino-3-(methylthio)thiocarbonyl-1,3-thiazolidineHCID 1214678445.2%

Reaction Steps

To a mixture of 2-(2-isopropylphenyl)imino-1,3-thiazolidine (0.22 g), carbon disulfide (0.09 g) and N,N-dimethylformamide (2 ml) was added under ice-cooling 60% sodium hydride (0.05 g). The mixture was stirred for 30 minutes. Methyliodide (0.17 g) was added thereto. The mixture was stirred at room temperature for 2 hours. To the mixture was added water (30 ml). The mixture was extracted with diethylether (60 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to give 2-(2-isopropylphenyl)imino-3-(methylthio)thiocarbonyl-1,3-thiazolidine (0.14 g, yield: 45%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818640B1
Source datasetuspto-grants-2004_11
ORD IDord-58942fa9fb1a41a0a37a4900cec8bee5
Source noteuspto-grants-2004_11