반응 #586105
ord-4d9a9293694846f2b7df498efe5dd4fb
반응 방정식
반응물
시약
반응 조건
후처리
- 1workup.STIRRINGThe mixture was stirred for a further 15 minutes
- 2workup.STIRRINGwhile stirring
- 3온도to warm to room temperature
- 4workup.STIRRINGwhile stirring
- 5workup.STIRRINGwas stirred for a further one hour
- 6기타the mixture obtained in this way
- 7온도was refluxed for 3 hours
- 8온도to cool to room temperature
- 9workup.STIRRINGwhile stirring
- 10기타The aqueous phase was then separated off from the organic phase
- 11추출the aqueous phase was extracted twice with diethyl ether
- 12건조dried over magnesium sulfate
- 13여과filtered
- 14workup.DISTILLATIONthe solvent was distilled off
- 15기타The residue obtained in this way
- 16workup.DISTILLATIONwas distilled at 119-139° C.
실험 절차
A mixture of 38.7 g (186 mmol) of 8-bromoquinoline in 250 ml of tetrahydrofuran was cooled to −80° C. and 74.4 ml of n-butyllithium (2.5 M in hexane, 186 mmol) were subsequently added while stirring. The mixture was stirred for a further 15 minutes and, while stirring, 49.9 g (186 mmol) of 2-methyl-3-(trimethylsilyloxy)cyclopent-2-enone were added. The mixture was allowed to warm to room temperature while stirring and was stirred for a further one hour. The reaction mixture was then hydrolyzed by means of a mixture of 40 g of ice and 30 ml of concentrated hydrochloric acid and the mixture obtained in this way was refluxed for 3 hours. The mixture was allowed to cool to room temperature while stirring and ammonia solution was added until the pH was 12. The aqueous phase was then separated off from the organic phase and the aqueous phase was extracted twice with diethyl ether. The organic phases were combined, dried over magnesium sulfate, filtered and the solvent was distilled off. The residue obtained in this way was distilled at 119-139° C. and 2×10−2 mbar to give 31.1 g (139.3 mmol, 74.9%) of 2-methyl-3-(8-quinolyl)cyclopent-2-enone.