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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051583Generated: October 25, 2026

Methyl iodide → N-(4-anilinophenyl)-N-(1,3-dimethyl-butyl)-dithiocarbamate methyl ester

https://huagongshe.com/reaction/2051583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
Reactant1,4-Benzenediamine, N-(1,3-dimethylbutyl)-N'-phenyl-HCID 13101—
ReactantSodium HydroxideHCID 14798—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-anilinophenyl)-N-(1,3-dimethyl-butyl)-dithiocarbamate methyl esterHCID 19832493—

Reaction Steps

N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine (26.8g, 0.10 mol) is dissolved in 100 mL tetrahydrofuran in a 250 mL, 3-neck round bottom flask. Carbon disulfide (7.6g, 0.10 mol) is added over 0.5 hours with the concurrent addition of an aqueous solution of sodium hydroxide (4.0g, 0.10 mol). When addition is complete, methyl iodide (14.2g, 0.10 mol) is added and the mixture refluxed for 1 hour. The solvent is then stripped off on a rotary evaporator and the residue extracted with methylene chloride. The extract is dried with MgSO4 and the solvent is again removed on the rotary evaporator to yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05019611
Source datasetuspto-grants-1991_05
ORD IDord-bd7ddee354044392b7d9546781f462db
Source noteuspto-grants-1991_05