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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616116Generated: October 30, 2026

Methyl chloroformate → 1-(3-Methoxycarbonyl-2-thioureido)-5-phenylsulfinyl-2-nitrobenzene

https://huagongshe.com/reaction/616116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantPotassium thiocyanateHCID 516872—
ReactantMethoxycarbonyl isothiocyanateHCID 552246—
Reactant5-(Benzenesulfinyl)-2-nitroanilineHCID 13035572—
SolventAcetoneHCID 180—
Product1-(3-Methoxycarbonyl-2-thioureido)-5-phenylsulfinyl-2-nitrobenzeneHCID 20371017—

Reaction Steps

A suspension of 5.2 g. of 1-amino-5-phenylsulfinyl-2-nitrobenzene in 50 ml. of acetone is treated at 20°-25° C with a solution of 100 ml. of methoxycarbonyl isothiocyanate (made from 0.125 mol. (each) of potassium thiocyanate and methylchloroformate) in acetone. After several days, the solvent is stripped off under vacuum and the residue triturated with ether. Recrystallization of the crude product from methanol-chloroform yields 1-(3-methoxycarbonyl-2-thioureido)-5-phenylsulfinyl-2-nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072696
Source datasetuspto-grants-1978_02
ORD IDord-24c8f623c81f489597ddaec554bbdc15
Source noteuspto-grants-1978_02