HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Phenylsulfanyl)acetaldehyde → N-Methyl-4-[2-[2-(phenylthio)ethylidene]hydrazino]benzenemethanesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Phenylsulfanyl)acetaldehyde | HCID 579732 | — |
| Reactant | 4-Hydrazino-N-methylbenzenemethanesulfonamide hydrochloride | HCID 14234263 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Methyl-4-[2-[2-(phenylthio)ethylidene]hydrazino]benzenemethanesulphonamide | HCID 67923715 | 78.9% |
Reaction Steps
A solution of (phenylthio)acetaldehyde (6.05 g) in absolute ethanol (180 ml) was added over 10 min to a solution of 4-hydrazino-N-methylbenzenemethanesulphonamide hydrochloride (10 g) in water (180 ml) with cooling. After addition of the aldehyde was complete, the mixture was stirred at 5° for a period of 14 h. The precipitated solid was filtered off, washed with water (200 ml), hexane (200 ml) and dried in vacuo to give the title compound (10.95 g), m.p. 110°-112°. T.l.c. (B) Rf 0.5 (KMnO4)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05037845 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-e14be7d50ca149a4b74fff06f34dbd4f |
| Source note | uspto-grants-1991_08 |