반응 #1714592
ord-6f40526e8e0d4b60a7e40450cf71a63d
반응 방정식
반응 조건
후처리
- 1workup.STIRRINGThe mixture was further stirred at room temperature for 24 hours
- 2온도was cooled to 0° C
- 3기타The reaction was terminated
- 4workup.ADDITIONby adding 1N hydrochloric acid, and hexane
- 5workup.ADDITIONwas added to the reaction liquid
- 6세척The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution
- 7건조The organic layer was dried over magnesium sulfate
- 8여과was filtered
- 9농축was concentrated under reduced pressure
- 10workup.DISTILLATIONThe concentrate was purified by distillation under reduced pressure
실험 절차
THF in a volume of 100 ml was added to 50 ml (100 mmol) of a 2 M THF solution of sodium cyclopentadienide, and the mixture was cooled to −78° C. A THF solution of 19.3 g (100 mmol) of 1-bromooctane was added thereto dropwise. Further, 11.4 g (100 mmol) of 1,3-dimethyl-2-imidazolidinone was added dropwise. The mixture was stirred at −78° C. The mixture was further stirred at room temperature for 24 hours and was cooled to 0° C. The reaction was terminated by adding 1N hydrochloric acid, and hexane was added to the reaction liquid. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and then with a saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, was filtered, and was concentrated under reduced pressure. The concentrate was purified by distillation under reduced pressure to give 6.7 g (37.5 mmol) of target n-octylcyclopentadiene. The compound was identified by GC-MS. GC-MS: 178 (MS).