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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21006Erstellt: 23. Oktober 2026

Dimethylformamide → 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone

https://huagongshe.com/de/reaction/21006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt3-chloro-N-(1-methyl-1-phenylethyl)benzamideHCID 47444761—
EduktHCID 178444656HCID 178444656—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinoneHCID 6849004389%

Reaktionsschritte

3-Chloro-N-(1-methyl-1-phenylethyl)benzamide (7.00 g, 25.6 mmol) was dissolved in THF (280 mL), and the solution was added with TMEDA (12.4 mL, 81.9 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 82.7 mL, 81.9 mmol) by drops at −78° C. for 40 minutes under argon atmosphere, followed by stirring at the same temperature for 2.5 hours. Then, the mixture was added with DMF (4.36 mL, 56.3 mmol) and warmed from −78° C. to room temperature over 2 hours. The reaction mixture was added with water, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by slurry using diisopropyl ether to obtain 4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, yield 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f45e4ddcaba84c37bb2475ecd5f8e92f
Quellennotizuspto-grants-2010_06