HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-amino-N-methyl-2-oxo-3-pentenesulfonamide | HCID 73663808 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamide | HCID 70045034 | — |
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 3.6 ml of benzyl bromide in 50 ml of dimethylformamide was treated with 6 g of potassium carbonate and the mixture was stirred intensively at room temperature for 9 hours. The product was firstly chromatographed on 300 g of silica gel with ethyl acetate as the elution agent and then recrystallized from isopropanol. There were obtained 3.4 g of 4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 115°-118°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742069 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-8cb9429ee40943b9b609b38b501c7db4 |
| Source note | uspto-grants-1988_05 |