HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Bromothiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-bromothiazole-5-carboxylate | HCID 2773502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Bromothiazole-5-carboxylic acid | HCID 2763210 | — |
Reaction Steps
A mixture containing 10 g. of 2-bromo-5-methoxycarbonylthiazole, 100 ml. of 10% aqueous sodium hydroxide and 200 ml. of methanol is stirred at 0° C for 5 minutes. The methanol is distilled off in vacuo and the resulting concentrate extracted twice with ethyl acetate. The remaining aqueous phase is acidified by the careful addition of dilute aqueous hydrochloric acid resulting in the formation of a precipitate which is then recovered by filtration and dried under vacuum yielding 2-bromo-5-carboxythiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089865 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-88dc2156b4c1436ba9bdcaf5319c1528 |
| Source note | uspto-grants-1978_05 |