HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371838Generated: October 26, 2026
18-Crown-6 → 3-(1,3-Dioxolan-2-YL)benzophenone
https://huagongshe.com/reaction/1371838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | (3-[1,3]Dioxolan-2-ylphenyl)phenylmethanol | HCID 10824966 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1,3-Dioxolan-2-YL)benzophenone | HCID 10515088 | — |
Reaction Steps
Combine (3-[1,3]dioxolan-2-ylphenyl)-phenyl-methanol (5.0 g, 18.5 mmol) and 18-crown-6 (160 mg, 0.6 mmol) in dichloromethane. Add potassium permanganate (8.8 g, 55.5 mmol). Heat to about 40° C. After 4 hours, cool to room temperature add water and sodium hydrogensulfite (6.0 g). Basify with a solution of 1N sodium hydroxide (about 60 ml) and extract with dichloromethane. Combine the organic layers and wash sequentially with distilled water and brine and then dry (Na2SO4), filter, and concentrate to give a residue. Chromatograph the residue eluting with EtOAc to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157488B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-6c79f5254bbc4c398986d677420a22b0 |
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| Source note | uspto-grants-2007_01 |
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