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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430102Generated: October 31, 2026

Potassium Permanganate → HCID 25059379, compound

https://huagongshe.com/reaction/1430102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PermanganateHCID 516875—
ReactantHCID 25059128HCID 25059128—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 25059379HCID 2505937977.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940769B2
Source datasetuspto-grants-2015_01
ORD IDord-c91ba93fbcbd417480bb5ed8ec7fbd98
Source noteuspto-grants-2015_01