HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanoic acid, 4-chloro-4-oxo-, ethyl ester → Ethyl 4-(2-thiazolyl)-4-oxobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanoic acid, 4-chloro-4-oxo-, ethyl ester | HCID 84648 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Trimethylsilylthiazole | HCID 588453 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(2-thiazolyl)-4-oxobutyrate | HCID 68499389 | — |
Reaction Steps
To a stirred solution of 2-trimethylsilanyl-thiazole (2.6 g, 16.53 mmol) in DCM (30 mL) is added a solution of 3-chlorocarbonyl-propionic acid ethyl ester (5.4 g, 32.81 mmol) in DCM (10 mL). The mixture is stirred overnight at room temperature. To the mixture is added 5% NaHCO3 (30 mL) and mixture is stirred at room temperature for 20 minutes. The organic layer is separated and the aqueous lay is extracted with DCM (2×50 mL). The combined organic layers are dried and the solvent removed. The residue is separated by column (methylene chloride) to give 4-oxo-4-thiazol-2-yl-butyric acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916819B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-12d7da43f945484daa8062389421f2d0 |
| Source note | uspto-grants-2005_07 |