HuagongsheHuagongshe Chemistry Print Report · For research reference only
Magnesium Carbonate → 5-Thiazolecarboxylic acid, 4-methyl-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Magnesium Carbonate | HCID 11029 | — |
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | Methanethioamide | HCID 3005587 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Thiazolecarboxylic acid, 4-methyl-, ethyl ester | HCID 298610 | — |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
Thioformamide (7.5 g, 122.72 mmol), ethyl 2-chloroacetoacetate (16.4 g, 99.52 mmol) and magnesium carbonate (20 g, 237.22 mmoL) were taken dioxane (100 mL) and heated at 110° C. for 4 hrs. The reaction mixture was cooled to room temperature and filtered to remove magnesium carbonate. The solvent was evaporated to dryness and the residue was taken in ether (200 mL) and washed successively with 0.5 M NaOH solution (200 mL×2) and saturated brine solution (100 mL) and dried over Na2SO4. It was filtered and evaporated to give 4-methyl-5-(ethoxycarbonyl)thiazole as an oil which was purified by silica gel column chromatography using hexanes:EtOAc (8:2, v/v) as a eluent; yield: 3.28 g (17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166625B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-91210069d59f45c1b0edaa997cdbb412 |
| Source note | uspto-grants-2007_01 |