تفاعل #624901
ord-4982a9d530f347d7b9be9e693cedc2a8
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.DISSOLUTIONto be dissolved
- 2workup.ADDITIONmixed solution with a magnetic stirrer
- 3workup.ADDITIONwas gradually added at room temperature in a nitrogen atmosphere
- 4درجة الحرارةThe reaction mixture was refluxed over 3 days
- 5workup.DISTILLATIONethyl acetate was distilled off under reduced pressure
- 6تركيزThe resultant concentrate
- 7workup.ADDITIONwas dropped into 100 mL of diethyl ether
- 8أخرىtetrahydrothiophene and trimethoxysilylpropyl iodide as by-products were removed
- 9أخرىThis purification
- 10workup.DISTILLATIONremaining diethyl ether was distilled off under reduced pressure
- 11workup.DISSOLUTIONby dissolving the resultant
- 12تركيزconcentrate in methanol
الإجراء التجريبي
2.0 g of tetrahydrothiophene and 18 g of ethyl acetate were charged into a 100 mL flask to be dissolved. While stirring the resultant mixed solution with a magnetic stirrer, to the mixed solution, a solution in which 9.9 g of trimethoxysilylpropyl iodide was dissolved in 24 g of ethyl acetate was gradually added at room temperature in a nitrogen atmosphere. The reaction mixture was refluxed over 3 days and therefrom, ethyl acetate was distilled off under reduced pressure. The resultant concentrate was dropped into 100 mL of diethyl ether and therefrom, tetrahydrothiophene and trimethoxysilylpropyl iodide as by-products were removed. This purification was repeated three times and then remaining diethyl ether was distilled off under reduced pressure, followed by dissolving the resultant concentrate in methanol to obtain a 30% methanol solution of trimethoxysilylpropyltetrahydrothiophene iodide.