تفاعل #49285

معادلة التفاعل

iodine

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

TMEDA

sodium thiosulfate

sec-butyllithium hexane

→

4-chloro-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone

المردود 85.0%

المذيبات

THF

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةwarmed from −78° C. to room temperature for 2.5 hours
2. 2
   استخلاصextracted with ethyl acetate
3. 3
   غسيلThe organic layer was washed with saturated brine
4. 4
   تجفيفdried over anhydrous sodium sulfate
5. 5
   أخرىThe solvent was evaporated under reduced pressure
6. 6
   أخرىthe residue was purified by flash column chromatography (chloroform/methanol=100/0, 85/15)

الإجراء التجريبي

4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, 22.7 mmol) was dissolved in THF (274 mL), and the solution was added with TMEDA (7.55 mL, 50.0 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 50.5 mL, 50.0 mmol) by drops at −78° C. over 20 minutes under argon atmosphere, followed by stirring at the same temperature for 2 hours. Then, the mixture was added with iodine (6.92 g, 27.3 mmol) and warmed from −78° C. to room temperature for 2.5 hours. The reaction mixture was added with 10% aqueous sodium thiosulfate solution and 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 flash column chromatography (chloroform/methanol=100/0, 85/15) to obtain 4-chloro-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone (8.22 g, yield 85%).

المصدر