HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430102Generated: October 31, 2026
Potassium Permanganate → HCID 25059379, compound
https://huagongshe.com/reaction/1430102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | HCID 25059128 | HCID 25059128 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 25059379 | HCID 25059379 | 77.4% |
Reaction Steps
0.40 g of {5-chloro-6-[4-(6-trifluoromethyl-1H-benzoimidazol-2-yl)-phenyl]-pyridin-3-yl}-methanol (28) (0.99 mmol) prepared in Example 16 was dissolved in 4 mL of pyridine and 2 mL of distilled water. 0.59 g of potassium permanganate (3.71 mmol) was added thereto, and reacted at 110° C. for 4 hours. Then, 0.59 g of potassium permanganate (3.71 mmol) and 2 mL of distilled water were added thereto, and reacted at 110° C. for 18 hours. The resultant was cooled to room temperature, and concentrated under reduced pressure. The aqueous layer was washed with ethyl acetate, pH 1 was adjusted with concentrated hydrochloric acid, and extracted with ethyl acetate several times. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was separated by column chromatography (eluting solvent: chloroform/methanol=10/1) to obtain 0.32 g of 5-chloro-6-[4-(6-trifluoromethyl-1H-benzoimidazol-2-yl)-phenyl]-nicotinic acid (yield 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940769B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-c91ba93fbcbd417480bb5ed8ec7fbd98 |
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| Source note | uspto-grants-2015_01 |
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