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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220395Erstellt: 26. Oktober 2026

Potassium Carbonate → Tert-butyl 1,3-dioxoisoindolin-2-yl(2-isopropoxyethyl)carbamate

https://huagongshe.com/reaction/220395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktN-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)(tert-butoxy)formamideHCID 801162—
Edukt2-Isopropoxyethyl MethanesulfonateHCID 18465045—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 1,3-dioxoisoindolin-2-yl(2-isopropoxyethyl)carbamateHCID 5818058983%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A round bottom flask charged with 2-isopropoxyethyl methanesulfonate (example 77A, 0.791 g, 4.34 mmol) in acetonitrile (21.70 mL) was stirred under an atmosphere of nitrogen. tert-Butyl 1,3-dioxoisoindolin-2-ylcarbamate (1.138 g, 4.34 mmol) was added along with potassium carbonate (2.399 g, 17.36 mmol) and benzyltriethylammonium chloride (0.198 g, 0.868 mmol). The reaction mixture was heated at 50° C. 24 h and cooled to rt over the weekend. The reaction mixture was diluted with ethyl acetate and water. The aqueous layer was extracted with ethyl acetate. The combined organics were washed with brine, dried over anhydrous sodium sulfate, vacuum filtered through a plug of silica gel and concentrated in vacuo. The crude oil was used without additional purification (1.26 g, 83% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202881B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-50c7568dcc72409cbf31471272f78f13
Quellennotizuspto-grants-2012_06