HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 4-Bromo-3-chloro-6-iodo-2-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Bromo-3-chloro-2-methylaniline hydrochloride | HCID 86654434 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-3-chloro-6-iodo-2-methylaniline | HCID 58306780 | 96.4% |
Reaction Steps
To a mixture of 4-bromo-3-chloro-2-methyl aniline hydrochloride (1.0 g), sodium acetate (0.5 g), and acetic acid (15 mL) was added N-iodosuccinimide (1.0 g) under water-cooling. The reaction mixture was stirred at room temperature for 3.5 hours. To the reaction mixture were added ethyl acetate and water, and alkalified by adding potassium carbonate. Then, a liquid-separation operation was carried out, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0-90:10) to obtain 4-bromo-3-chloro-6-iodo-2-methylaniline (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598355B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-5c7205a44212413690f5446e8c8d412c |
| Source note | uspto-grants-2013_12 |