HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-(4-Chloro-2-methoxyphenyl)-4-methylthiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(4-chloro-2-methoxyphenyl)-4-methylthiazole-5-carboxylate | HCID 68642456 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Chloro-2-methoxyphenyl)-4-methylthiazole-5-carboxylic acid | HCID 68642048 | 97.3% |
Reaction Steps
Ethyl 2-(4-chloro-2-methoxyphenyl)-4-methylthiazole-5-carboxylate (4.83 g, 15.5 mmol) prepared in the Step 7-1-3 was suspended in ethanol (30 ml), 1 mol/l of sodium hydroxide (30 ml) was added thereto, and the mixture was heated under reflux for 1.5 hours. After being allowed to cool, the mixture was neutralized with hydrobromic acid, then separated by filtration and washed with water. The washed product was subjected to through circulation drying to give the title compound (4.28 g, 97%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200008B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-be7a5f609fa6480c945041ae81283da5 |
| Source note | uspto-grants-2015_12 |