HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Benzothiazole-6-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl benzo[d]thiazole-6-carboxylate | HCID 10512520 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzothiazole-6-carboxylic acid | HCID 601670 | 98% |
Reaction Steps
Ethyl benzothiazole-6-carboxylate (1.30 g, 6.28 mmol) prepared in the Step 36-1-2 was suspended in ethanol (10 ml) and a 1 mol/L sodium hydroxide aqueous solution (10 ml), and the mixture was heated under reflux for 40 minutes. After the mixture was allowed to cool, concentrated hydrobromic acid was added to the mixture, and the resulting mixture was adjusted to pH 4. The precipitate was separated by filtration, washed with water, and then subjected to through circulation drying to give the title compound (1.10 g, 98%) as a light-brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200008B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-bcb865b48d1d43babfcd1070fbaed53a |
| Source note | uspto-grants-2015_12 |