تفاعل #1714592
ord-6f40526e8e0d4b60a7e40450cf71a63d
معادلة التفاعل
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المعالجة
- 1workup.STIRRINGThe mixture was further stirred at room temperature for 24 hours
- 2درجة الحرارةwas cooled to 0° C
- 3أخرىThe reaction was terminated
- 4workup.ADDITIONby adding 1N hydrochloric acid, and hexane
- 5workup.ADDITIONwas added to the reaction liquid
- 6غسيلThe organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution
- 7تجفيفThe organic layer was dried over magnesium sulfate
- 8ترشيحwas filtered
- 9تركيزwas concentrated under reduced pressure
- 10workup.DISTILLATIONThe concentrate was purified by distillation under reduced pressure
الإجراء التجريبي
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).