反応 #516884
ord-d8c478f2b6bb4e87be67570514c610ae
反応条件
後処理
- 1workup.ADDITIONwas added slowly over a period of 15 minutes
- 2workup.STIRRINGthe mixture was stirred for an additional 2 hours at room temperature
- 3ろ過The product was filtered
- 4洗浄washed with 25 ml of ice cold 95% ethanol
- 5その他A small amount of product was recovered from the filtrate with the addition of 75 ml
- 6workup.DISTILLATIONdistilled water
- 7その他Finally, the product was recrystallized from 120 ml of acetone giving 21.8 g of cholesteryl bromide (yield, 75%) with a melting point of 93-95% C
- 8その他(lit 97-98° C.)
実験手順
Cholesterol, (25 g, 64.6 mmol) was dissolved in 10 ml of dimethylaniline (78.9 mmol) and 5 ml of chloroform. While stirring on ice; small quantities of thionyl bromide (6 ml, 77.6 mmol) dissolved in 20 ml of cold chloroform was added slowly over a period of 15 minutes. After the addition of thionyl bromide was complete, the mixture was stirred for an additional 2 hours at room temperature. The resulting solution was poured into 200 ml of ice cold 95% ethanol and left on ice for 2 hour until crystallization was complete. The product was filtered and washed with 25 ml of ice cold 95% ethanol. A small amount of product was recovered from the filtrate with the addition of 75 ml distilled water followed by refrigeration. Finally, the product was recrystallized from 120 ml of acetone giving 21.8 g of cholesteryl bromide (yield, 75%) with a melting point of 93-95% C. (lit 97-98° C.). The identity of the product was confirmed with mass spectrometry (EI) which showed an intense peak with an m/z of 448, corresponding to the molecular ion (M+°) of cholesteryl bromide. Also, the bromide molecular weight pattern characteristic of the two different isotopes of bromine (79Br:81-Br,1:1) was observed.