반응 #531525
ord-18eed096bc914123a9135fe54c5fc26c
반응 방정식
반응물
시약
없음
용매
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타To a 0° C.
- 2workup.ADDITIONis then added to 250 ml
- 3건조The ether phase is dried over magnesium sulfate
- 4기타evaporated
- 5기타The residue is purified via column chromatography on 200 g
- 6세척of silica gel eluted with 50% ether-cyclohexane
실험 절차
To a 0° C. solution of 7.0 mmols. of 3-phenylpropylmagnesium bromide in 7 ml. of tetrahydrofuran is slowly added a solution of 2.48 g. (5.0 mmols) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidone in 10 ml. of tetrahydrofuran. The resultant mixture is stirred for one hour and is then added to 250 ml. of saturated ammonium chloride-250 ml. ether. The ether phase is dried over magnesium sulfate and evaporated. The residue is purified via column chromatography on 200 g. of silica gel eluted with 50% ether-cyclohexane to yield the title compound.