HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777332Generated: November 1, 2026
Potassium Permanganate → 3-Chloro-4-cyclohexylbenzoic acid
https://huagongshe.com/reaction/1777332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 1-(3-Chloro-4-cyclohexylphenyl)ethanone | HCID 10900646 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Chloro-4-cyclohexylbenzoic acid | HCID 20310416 | — |
Reaction Steps
An aqueous alkaline solution of potassium permanganate (2.94 g, 0.0186 mol; in 22 mL 12% aqueous sodium hydroxide) is added to solution of 1-(3-chloro-4-cyclohexylphenyl)ethanone (2.2 g, 0.0093 mol) in dioxane (11 mL). The reaction mixture is stirred at 80° C. temperature for 2 hrs. It is then filtered and the filtrate is washed with diethyl ether (2×10 mL). The pH of the aqueous layer is adjusted to 1-2 by using 6N hydrochloric acid. It is extracted in ethyl acetate (3×15 mL). Combined organic layer is dried over sodium sulfate and concentrated to get the crude, which is purified using column chromatography (230-400 mesh; ethyl acetate:n-hexane, 1:3) to yield 3-chloro-4-cyclohexyl benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266867B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b661e3883d424e9fa748ca86e317c077 |
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| Source note | uspto-grants-2016_02 |
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