Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2-chloro-1-isothiocyanato-4-nitrobenzene | HCID 2757736 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19025427 | HCID 19025427 | 80.8% |
Reaction Steps
To a stirred solution of 60.0 g (0.280 mole) of 2-chloro-4-nitrophenyl isothiocyanate in 500 ml of ethanol was added 12.9 g (0.280 mole) of methylhydrazine. This mixture was heated and was stirred at 65° C. for approximately 18 hours. The mixture was then heated to reflux and was cooled. A solid had formed and was collected by filtration. The filter cake was rinsed with aqueous ethanol and was dried under reduced pressure to yield 59.0 g of 4-(2-chloro-4-nitrophenyl)-2-methyl-3-thiosemicarbazide, mp 164°-167° C. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05108486 |
|---|
| Source dataset | uspto-grants-1992_04 |
|---|
| ORD ID | ord-e0800a43804c4bc9a5f3dc7c01df1a49 |
|---|
| Source note | uspto-grants-1992_04 |
|---|