HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-(1-Phenylprop-1-ene-2-sulfonyl)piperidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-(Diphenylcarbamoyl)-1-phenylprop-1-ene-2-sulfonamide | HCID 54322426 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(1-Phenylprop-1-ene-2-sulfonyl)piperidine-1-carboxamide | HCID 54049334 | — |
Reaction Steps
A solution of 1.9g. of N-(N,N-diphenylcarbamoyl)-1-phenylpropene-2-sulfonamide and 1.7g of piperidine in 10ml. of N,N-dimethylformamide is maintained at ca. 95°C. for 6 hours. It is then cooled to ambient temperature, and 100 ml. of ether is added. The mixture is extracted with 50 ml. of water, and then the water extract is acidified using concentrated hydrochloric acid. This causes the crude product to precipitate. It is filtered off, and then it is recrystallized from a mixture of acetone and water giving 670 mg. of N-(piperidinocarbonyl)-1-phenylpropene-2-sulfonamide, m.p. 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983107 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-c9d6466482fd4241a47070f98fe79e18 |
| Source note | uspto-grants-1976_09 |