反応 #833542
ord-7d0e5610022d4caa842357aab5998499
反応方程式
溶媒
反応条件
後処理
- 1workup.ADDITIONAt the end of the addition reaction mixture
- 2workup.STIRRINGAfter additional 10 min of stirring
- 3workup.ADDITIONwere added
- 4温度The resulted mixture was refluxed for 15 hrs
- 5温度to cool to RT
- 6温度Additional refluxing for 3 hrs
- 7その他required for reaction completion
- 8その他Resulted
- 9その他reaction mixture
- 10温度was cooled with ice bath
- 11workup.ADDITIONpoured
- 12workup.STIRRINGwith stirring, into a vessel
- 13抽出extracted with 300 ml of ether
- 14その他The organic layer was separated
- 15洗浄washed with 3×150 ml of water, 150 ml of saturated NaCI aqueous solution
- 16乾燥dried over sodium sulfate
- 17その他After removal of ether material
- 18その他was purified by recrystallization from n-hexane
- 19ろ過filtering out
- 20その他drying over high vacuum
実験手順
Under inert atmosphere 2.0 gr of sodium metal suspension (40% in mineral oil) were slowly added to 100 ml of dry methanol at 0° C. At the end of the addition reaction mixture was stirred for 10 min at RT and 1.75 ml (21.58 mmole) of thioacetic acid were added. After additional 10 min of stirring, 30 ml degassed methanolic solution of 6.1 gr (18.19 mmole) of 16bromohexadecanoic acid were added. The resulted mixture was refluxed for 15 hrs, after which, allowed to cool to RT and 50 ml of degassed 1.0 M NaOH aqueous solution were injected. Additional refluxing for 3 hrs required for reaction completion. Resulted reaction mixture was cooled with ice bath and poured, with stirring, into a vessel containing 200 ml of ice water. This mixture was titrated to pH=7 by 1.0 M HCl and extracted with 300 ml of ether. The organic layer was separated, washed with 3×150 ml of water, 150 ml of saturated NaCI aqueous solution and dried over sodium sulfate. After removal of ether material was purified by recrystallization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product was obtained.