HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methoxycarbonyl isothiocyanate → 4-n-Butylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methoxycarbonyl isothiocyanate | HCID 552246 | — |
| Reactant | 4-(Butylsulfanyl)-2-nitroaniline | HCID 11031561 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-n-Butylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene | HCID 20371054 | — |
Reaction Steps
2.5 G. of 1-amino-4-n-butylthio-2-nitrobenzene (alternatively prepared according to Example II) is dissolved in 25 ml. acetone and treated at room temperature with 3 g. methoxy carbonyl isothiocyanate. The mixture is left overnight, stripped under vacuum and the residue triturated with methanol and recrystallized from methanol to yield pure 4-n-butylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072696 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-0878a5a5fd5b4eec8345d997b702a243 |
| Source note | uspto-grants-1978_02 |