HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309336Generated: October 27, 2026
Methanethiol → Methyl benzoyldithiocarbamate
https://huagongshe.com/reaction/2309336
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Benzoyl thiocyanate | HCID 13203561 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl benzoyldithiocarbamate | HCID 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 acetronitrile 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04695311 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-2253f9b5ce784b2595b82e9ae1beb076 |
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| Source note | uspto-grants-1987_09 |
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