반응 #56995
ord-6a6ff2f7dfb94c5b87db587bf52ef7fa
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용매
반응 조건
후처리
- 1온도the mixture was heated
- 2온도to reflux for 3 h. (
- 3기타quenched with sat. NH4Cl solution
- 4여과The mixture was filtered
- 5기타partitioned between brine and diethyl ether
- 6기타The organic layer was removed
- 7건조dried over Na2SO4
- 8여과filtered
- 9농축concentrated under vacuum
- 10기타The oil was purified by chromatography on SiO2 with 20% EtOAc
실험 절차
The alcohol (Intermediate D3, 16 mmol) in THF (30 mL) at 0° C. was treated with isobutyl magnesium bromide (40 mmol). The catalyst, 1,3-bis(diphenylphosphino)propane nickel (II) chloride (0.75 mmol) (NiCl2dppp) was added in one portion and the mixture was heated to reflux for 3 h. (see: Organ et al. J. Org. Chem. 1997, 62, 1523, incorporated herein by reference). The reaction mixture was cooled to rt and quenched with sat. NH4Cl solution. The mixture was filtered and partitioned between brine and diethyl ether. The organic layer was removed and dried over Na2SO4, filtered and concentrated under vacuum. The oil was purified by chromatography on SiO2 with 20% EtOAc:Hx to yield 2-isobutyl-cyclopent-2-enol (Intermediate D4). Use of 2-isobutyl-cyclopent-2-enol (Intermediate D4) in Method A produced 4-(2-isobutyl-cyclopent-2-enylmethyl)-1,3-dihydro-imidazole-2-thione (Compound 20).