HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → Ethyl (2-propyl-1,3-thiazol-5-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Butanethioamide | HCID 12454243 | — |
| Reactant | Ethyl 2-bromo-4-oxo-butyrate | HCID 18668033 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Ethyl (2-propyl-1,3-thiazol-5-yl)acetate | HCID 54320013 | 73.3% |
Reaction Steps
A mixture of 20.6 g of ethyl 2-bromo-4-oxo-butyrate, 10.9 g of thiobutyramide and 400 ml of dichloroethane was refluxed under a nitrogen atmosphere which recycling the dehydrated condensate. The mixture was cooled and then mixed with 45 ml of a saturated sodium bicarbonate aqueous solution. The mixture was decanted and the organic phase was dried and evaporated to dryness. The liquid residue was chromatographed over silica gel and elution with a 8-2 cyclohexane-benzene mixture yielded 15.4 g of ethyl 2-propyl-5-thiazole-acetate. The IR spectrum in CHCl3 showed an ester carbonyl at 1737cm-1 and C=C at 1536cm-1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053618 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-7972fdc278954c5f9728ea362ee147ab |
| Source note | uspto-grants-1977_10 |