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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 589321Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/589321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPotassium PermanganateHCID 516875—
Edukt2-(Undec-10-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 22044522—
EduktSodium BisulfiteHCID 23665763—
KatalysatorTrioctylmethylammonium chlorideHCID 21218—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
Produkt10-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)decanoic acidHCID 1362263961%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09233115B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-0682b115e54c4959a645dc54984e67f5
Quellennotizuspto-grants-2016_01