HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-amino-N-methyl-2-oxo-3-pentenesulfonamide | HCID 73663808 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamide | HCID 73663809 | — |
Reaction Steps
In accordance with the procedure described in Example 7, a solution of 3.8 g of 4-amino-N-methyl-2-oxo-3-pentenesulfonamide and 2.5 ml of allyl bromide in 50 ml of dimethylformamide was treated with 6 g of potassium carbonate and the mixture was stirred intensively at room temperature for 7 hours. The product was firstly chromatographed on 300 g of silica gel with methylene chloride/ethyl acetate (4:1) as the elution agent and then recrystallized from methylene chloride/ether. There were obtained 3.3 g of N-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 86°-89°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742069 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-2600abd8c1624937bae69247c52d2514 |
| Source note | uspto-grants-1988_05 |