HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605493Generated: October 25, 2026
Acetic Acid → 10-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)decanoic acid
https://huagongshe.com/reaction/605493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dione | HCID 22044522 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Trioctylmethylammonium chloride | HCID 21218 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 10-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)decanoic acid | HCID 13622639 | 61% |
Reaction Steps
A solution of 2-undec-10-enyl-1,3-dioxo-1,3-dihydroisoindole (2 g, 6.68 mmol) of Step 1 and Aliquat® 336 (0.2 g) in a mixture of hexane (20 ml) and acetic acid (6 ml) was added dropwise to a solution of potassium permanganate (2.76 g, 20 mmol) in water (28 ml) while cooling at 0° C. The reaction mixture was stirred at room temperature for 7 hours, then an aqueous solution of sodium bisulfite was added until disappearance of the purple colour. The mixture was then extracted with ethyl acetate and the organic phase was dried over sodium sulfate and concentrated. The residue was purified by silica gel column chromatography eluting with 2:1 hexane:ethyl acetate mixture. The product was obtained as a white solid (1.29 g, 61% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915236B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-f125ec56c94647bfae156a499abdfa0d |
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| Source note | uspto-grants-2011_03 |
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