HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258762Generated: October 30, 2026
Acetonitrile → 4-Ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene
https://huagongshe.com/reaction/258762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 1-Amino-4-ethylthio-2-nitrobenzene | HCID 20372045 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene | HCID 20372053 | 39.2% |
Reaction Steps
A mixture of dry potassium thiocyanate (25.65 g.) and acetonitrile (320 ml.) was cooled to 10° C. and treated during 5 minutes with methyl chloroformate (25.0 g.). The mixture was stirred at room temperature for 2 hours. 1-Amino-4-ethylthio-2-nitrobenzene (22.45 g.) was then added to the mixture at 10°-15° C. The suspension was stirred for 3 hours at room temperature and allowed to stand overnight. It was then poured into water (1.6 liters) and the solid which precipitated was filtered off, washed with water and recrystallised from a mixture of methanol and ethanol, to give 4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene (14.0 g.), m.p. 152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04034107 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-c37ed3ac3f494bd9bfe7ce054493466d |
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| Source note | uspto-grants-1977_07 |
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