HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Ethyl 2-bromo-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl 2-aminothiazole-4-carboxylate | HCID 73216 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-bromo-1,3-thiazole-4-carboxylate | HCID 353965 | 57.6% |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
A solution of 30 g (174.3 mmol) ethyl-2-aminothiazole-4-carboxylate [prepared as in Example 1a)] in a mixture of 100 ml HBr (65%) and 100 ml of water was cooled to -15° C. and a solution of 12.03 g (174.3 mmol) sodium nitrite in 40 ml water was added over a period of 30 minutes and the mixture stirred for another 30 minutes at -15° C. After warming to room temperature, the solid was collected, washed with 50 ml cold water and dried to give 23.7 g (57.6%) ethyl-2-bromothiazole-4-carboxylate m.p. 63°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693594 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-a477c547d44145c68efc504b379d6707 |
| Source note | uspto-grants-1997_12 |