HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Bromo-5-(trifluoromethyl)pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Amino-5-(trifluoromethyl)pyridine | HCID 735862 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-5-(trifluoromethyl)pyridin-2-amine | HCID 13064155 | 78.5% |
Reaction Steps
In a 100 ml four necked flask equipped with the same equipments as those used in Example 3 were placed 3 g of 2-amino-5-trifluoromethylpyridine and 30 ml of acetic acid to provide a homogeneous solution. 4.4 g of bromine was dropwise added thereto while cooling the flask with ice water at 10° to 20° C., and after completion of the dropwise addition, the mixture was reacted for 1 hour. The reaction product was poured into 200 ml of water, washed with an aqueous solution of sodium thiosulfate and extracted with methylene chloride. The methylene chloride layer was dried over anhydrous sodium sulfate, and the solvent was evaporated off. The solid thus obtained was washed with n-hexane to obtain 3.5 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04349681 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-fa8e818a9a8b4f8d9aedfb219feeefc4 |
| Source note | uspto-grants-1982_09 |