HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728132Generated: November 1, 2026
Potassium Carbonate → HCID 10083053, compound
https://huagongshe.com/reaction/728132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(4-Aminobenzyl)pyridine | HCID 459525 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10083053 | HCID 10083053 | 14.1% |
Reaction Steps
A solution of 2-(4-aminobenzyl)pyridine (4.5 g) and ammonium thiocyanate (3.7 g) in acetic acid (50 ml) was stirred at ambient temperature for 1 hour. A solution of bromine (1.3 ml) in acetic acid (5 ml) was dropwise added thereto at 10° to 15° C. under stirring and the resulting mixture was stirred at 10° to 20° C. for 1 hour. A mixture of ethyl acetate and water was added to the reaction mixture and the mixture was adjusted to pH 7.5 with potassium carbonate. An insoluble material was filtered off and the filtrate was separated. The resulting organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated and triturated with ethyl acetate. The precipitate was collected by filtration and dried to give 6-[(2-pyridyl)methyl]-2-aminobenzothiazole (0.83 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047411 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-e0167ebf1aa54bb4804638296c761734 |
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| Source note | uspto-grants-1991_09 |
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