HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 13853976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Thiazolidinone | HCID 637591 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13853976 | HCID 13853976 | — |
Reaction Steps
A solution of 4-oxothiazolidine (50 g) in tetrahydrofuran (900 ml) was added dropwise to a suspension of sodium hydride (60% dispersion in mineral oil) (22.6 g) in tetrahydrofuran (850 ml) at room temperature and the mixture was allowed to warm up to reflux temperature. After the mixture was refluxed for an additional 30 minutes, ethyl bromoacetate (60 ml) was added dropwise under that condition. The mixture was refluxed further 1 hour and then cooled. Insoluble materials were removed by filtration. The filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography by eluting with chloroform to give ethyl 4-oxo-3-thiazolidinylacetate (78.5 g) as light brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764514 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-f55b41624f3049e8a1e0f3dc130644a9 |
| Source note | uspto-grants-1988_08 |