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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354009Generated: October 26, 2026

Acetic Acid → 10-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)decanoic acid

https://huagongshe.com/reaction/1354009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium PermanganateHCID 516875—
Reactant2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 22044522—
ReactantSodium BisulfiteHCID 23665763—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product10-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)decanoic acidHCID 1362263961%

Reaction Conditions

Temperature0 °C

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). M.p. 58–60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223745B2
Source datasetuspto-grants-2007_05
ORD IDord-fa51d15a78e54c8aae2ef4e92746a5d9
Source noteuspto-grants-2007_05