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HRID 560128作成日:2026年10月25日

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

https://huagongshe.com/reaction/560128

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-cyclopent-2-enolHCID 11137462—
反応物HCID 178418816HCID 178418816—
触媒Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
溶媒TetrahydrofuranHCID 8028—
生成物2-Isobutyl-cyclopent-2-enolHCID 21986210—

反応手順

The alcohol (Intermediate D3, 16 mmol) in THF (30 mL) at 0 EC 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063086B2
出典データセットuspto-grants-2011_11
ORD IDord-3d3b600fb25f4a6d999db890f9c3252b
出典メモuspto-grants-2011_11