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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9258생성일: 2026년 10월 24일

2-Bromo-cyclopent-2-enol → 2-Isobutyl-cyclopent-2-enol

https://huagongshe.com/ko/reaction/9258

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-cyclopent-2-enolHCID 11137462—
반응물HCID 178418816HCID 178418816—
촉매Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
용매TetrahydrofuranHCID 8028—
생성물2-Isobutyl-cyclopent-2-enolHCID 21986210—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091232B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-61a939bb8ae141e4bb2ed9c3a947327d
출처 메모uspto-grants-2006_08