HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → 1-(3-Methoxycarbonyl-2-thioureido)-5-phenylsulfinyl-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Methoxycarbonyl isothiocyanate | HCID 552246 | — |
| Reactant | 5-(Benzenesulfinyl)-2-nitroaniline | HCID 13035572 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(3-Methoxycarbonyl-2-thioureido)-5-phenylsulfinyl-2-nitrobenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072696 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-24c8f623c81f489597ddaec554bbdc15 |
| Source note | uspto-grants-1978_02 |