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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20905Erstellt: 23. Oktober 2026

Diisopropylcarbodiimide → 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl Ester

https://huagongshe.com/de/reaction/20905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylcarbodiimideHCID 12734—
EduktPentafluorophenolHCID 13041—
Edukt1,3-Dihydro-1,3-dioxo-2H-isoindole-2-hexanoic acidHCID 78185—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl EsterHCID 59347289101,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Referring to scheme 12, compound 41a (13.3 g, 51 mmol) was dissolved in anhydrous dichloromethane (40 mL) and cooled to 0° C. under argon. To the solution were added diisopropyl carbodiimide (6.31 g, 7.7 mL, 50 mmol) and pentafluoro phenol (42, 9.2 g, 50 mmol). After overnight the reaction mixture was evaporated to dryness. To the residue ethyl acetate (100 mL) was added and the filtered to remove diisopropyl urea. The precipitate was washed with ethyl acetate (50 mL). The combined organic layer was washed with saturated sodium bicarbonate and water. The organic layer was dried over sodium sulfate, filtered and evaporated to dryness. Compound 43a (Rf=0.8 in 10% EtOAc/Hexane, 21.65 g, 92%) was obtained, which was directly used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745608B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-943b155b15a6447a8e8a5b8587520e9e
Quellennotizuspto-grants-2010_06