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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1766013Erstellt: 26. Oktober 2026

Triethylamine → 2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1766013

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt4-ChlorobenzenepropanolHCID 221971—
EduktPhthalimide potassium saltHCID 24194345—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dioneHCID 1784890792,3%

Reaktionsschritte

Mesyl chloride (2.10 ml, 27.1 mmol) was added to a solution of 3-(4-chlorophenyl)propyl alcohol (4.6 g, 27 mmol) obtained in 1) above and triethylamine (3.78 ml, 27.1 mmol) in tetrahydrofuran (100 ml) at 0° C. and stirred at room temperature for 30 minutes. Water was added to the reaction mixture which was then extracted with ethyl acetate. The extract was washed with an aqueous saturated NaCl solution and dried over anhydrous magnesium sulfate. After the solvent was distilled away under reduced pressure, the reaction mixture and potassium phthalimide (5.02 g, 27.1 mmol) were dissolved in dimethylformamide and heated at 80° C. for 10 hours under stirring. 8 N aqueous sodium hydroxide was added to the resultant solution which was then extracted with ethyl acetate. The extract was washed with an aqueous saturated NaCl solution and dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, whereby 7.47 g 2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dione was obtained as solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07229986B2
Quelldatensatzuspto-grants-2007_06
ORD IDord-ad7a9c8a03a7489e8fad45aebf568bb8
Quellennotizuspto-grants-2007_06