تفاعل #49361

معادلة التفاعل

diisopropylethylamine

chloromethyl methyl ether

hydrochloric acid water

sodium hydroxide

diisopropylethylamine

chloromethyl methyl ether

3-Acetoxy-N-(1-methyl-1-phenylethyl)benzamide

→

3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamide

المردود 84.0%

المذيبات

water

methanol

ظروف التفاعل

المعالجة

1. 1
   استخلاصextracted with ethyl acetate
2. 2
   غسيلThe organic layer was washed with saturated brine
3. 3
   تجفيفdried over anhydrous sodium sulfate
4. 4
   أخرىThe solvent was evaporated under reduced pressure
5. 5
   workup.DISSOLUTIONThe residue was dissolved in dichloromethane (190 mL)
6. 6
   درجة الحرارةcooling
7. 7
   درجة الحرارةThen, the reaction mixture was warmed to room temperature
8. 8
   workup.STIRRINGstirred for 2 hours
9. 9
   workup.STIRRINGby further stirring for 2 hours
10. 10
    استخلاصextracted with chloroform
11. 11
    غسيلThe organic layer was washed with saturated brine
12. 12
    تجفيفdried over anhydrous sodium sulfate
13. 13
    أخرىThe solvent was evaporated under reduced pressure
14. 14
    أخرىThe residue was purified by flash column chromatography (chloroform/methanol=100/0, 99/1)

الإجراء التجريبي

3-Acetoxy-N-(1-methyl-1-phenylethyl)benzamide (9.57 g, 32.2 mmol) was dissolved in methanol (190 mL), and the solution was added with 4 mol/L sodium hydroxide solution (32.2 mL), followed by stirring at room temperature for 20 minutes. The reaction mixture was added with 1 mol/L hydrochloric acid water to adjust the pH to 7, 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. The residue was dissolved in dichloromethane (190 mL), and the solution was added with diisopropylethylamine (16.8 mL, 96.6 mmol) and chloromethyl methyl ether (3.70 mL, 48.3 mmol) under ice-cooling. Then, the reaction mixture was warmed to room temperature and stirred for 2 hours. The mixture was added with diisopropylethylamine (5.60 mL, 32.2 mmol) and chloromethyl methyl ether (1.20 mL, 15.8 mmol), followed by further stirring for 2 hours. The reaction mixture was added with water and extracted with chloroform. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (chloroform/methanol=100/0, 99/1) to obtain 3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamide (8.09 g, yield 84%).

المصدر