HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isobutyl Ketone → 3-(2-Nitrophenylmethyl)-2-thiazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Thiazolidinone | HCID 97431 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Nitrobenzylbromide | HCID 11356361 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Nitrophenylmethyl)-2-thiazolidinone | HCID 131964 | 37% |
Reaction Steps
A mixture containing 3.09 g (0.03 mol) of 2-thiazolidinone, 11.2 g of potassium carbonate, 1.8 g of potassium hydrogen carbonate, 0.5 ml of water, 30 ml of methyl isobutyl ketone and 6.5 g (0.03 mol) of nitrobenzyl bromide is refluxed for 6 hours, then cooled down and thoroughly mixed with 50 ml of water. The mixture is filtered and the clear filtrate is separated. The organic phase is washed with 10 ml of water, dried and evaporated. The oily residue is recrystallized from ethanol to give 2.65 g (37.0%) of the title compound, m.p.: 92°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937252 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-8e5cfbeb71f34778bf07aa59cb31cada |
| Source note | uspto-grants-1990_06 |