HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamide → N,N-Dimethyl-1H-indole-5-ethanesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamide | HCID 54171503 | — |
| Catalyst | Palladium monoxide | HCID 5083724 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N,N-Dimethyl-1H-indole-5-ethanesulphonamide | HCID 13475761 | 73.1% |
Reaction Steps
A solution of the product of Stage (i) (3.8 g) in ethanol (400 ml) was hydrogenated at room temperature and pressure over 10% palladium oxide on charcoal (50% aq. paste, 0.5 g), for 2 h. The catalyst was filtered off and replaced with a fresh batch (50% aq. paste, 0.5 g) and hydrogenation continued for a further 1 h. The catalyst was filtered off and the filtrate evaporated in vacuo to give a solid (2.8 g) which was recrystallised from a mixture of ethyl acetate and hexane to give the title compound as a solid (2.0 g) m.p. 125°-127°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994483 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-4ad1340e93b541ef9f1eaa45b4a634a6 |
| Source note | uspto-grants-1991_02 |