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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980770Generated: October 27, 2026

Methanethiol → Methyl benzoyldithiocarbamate

https://huagongshe.com/reaction/1980770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
Reactant2-Nitrobenzoyl chlorideHCID 11875—
ReactantPotassium thiocyanateHCID 516872—
ReactantBenzoyl thiocyanateHCID 13203561—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
ProductMethyl benzoyldithiocarbamateHCID 12497894—

Reaction Steps

Thus, in the reaction of Equation 43a, 2-nitrobenzoyl chloride LVII is reacted with potassium thiocyanate in a solvent such as toluene or acetonitrile at reflux for 0.2 to 5 hours; the resultant benzoyl thiocyanate is then reacted with excess methanol, ethanol or methyl mercaptan at 25° to 80° C. for 0.2 to 5 hours to form an O-alkyl benzoylthiocarbamate or methyl benzoyldithiocarbamate of Formula (LVIII). In reaction 43b, LVIII is reacted with sodium methoxide and methyl iodide in methanol at 0° to 25° C. for 1 to 5 hours to form a dialkyl benzoyliminothiocarbonate or dimethyl benzoyliminodithiocarbonate of Formula (LIX). And in reaction 43c, LIX is reacted with hydroxylamine in methanol or ethanol at 0° to 25° C. for about 10 to 96 hours to form Xm'.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511392
Source datasetuspto-grants-1985_04
ORD IDord-fa2900402cfd4ce5baae8c22d3e458ef
Source noteuspto-grants-1985_04