HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(5-Bromothiazol-2-yl)-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Acetamido-5-bromo-1,3-thiazole | HCID 350260 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(5-Bromothiazol-2-yl)-N-methylacetamide | HCID 67147803 | 36.8% |
Reaction Steps
1.9 g (14 mmol) of potassium carbonate and 3.94 ml (63.3 mmol) of methyl iodide are added to a solution of 2.8 g (12.7 mmol) of N-(5-bromothiazol-2-yl)acetamide in 50 ml of acetone. The reaction medium is refluxed for 3 hours. After addition of water, the reaction medium is extracted with ethyl acetate. The organic phase is washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 7/3 heptane/ethyl acetate mixture. 1.1 g (36%) of N-(5-Bromothiazol-2-yl)-N-methylacetamide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968560B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-be10c38530f643d498acdaac86883439 |
| Source note | uspto-grants-2011_06 |