HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonamide → 1,3-Dimethyl-5-tosyl-5,6-dihydro-4H-thieno[3,4-c]pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Bis(chloromethyl)-2,5-dimethylthiophene | HCID 288399 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Dimethyl-5-tosyl-5,6-dihydro-4H-thieno[3,4-c]pyrrole | HCID 18947057 | 63.6% |
Reaction Steps
A solution of 10 g (0.048 mol) of 3,4-bis(chloromethyl)-2,5-dimethylthiophene and 8.22 g of p-toluenesulphonamide in 600 ml of dry dimethylformamide is added dropwise, over 6 h, to a stirred suspension, heated to 100°-110° C., of 180 g of potassium carbonate in 900 ml of dimethylformamide. After the end of the addition, the mixture is maintained at the same temperature for 30 min, and then filtered. The solid is washed with dimethylformamide. The filtrate is concentrated under vacuum, and the residue is treated with 100 ml of ethanol, and filtered. The solid residue remaining is washed with ethanol and dried. 9.39 g of product are obtained. Melting point: 163°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380742 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-32ddc447f8a04f45a562d00df4e39c31 |
| Source note | uspto-grants-1995_01 |