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HRID 2099387作成日:2026年10月27日

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

https://huagongshe.com/reaction/2099387

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US07569584B2
出典データセットuspto-grants-2009_08
ORD IDord-4b965e6d0ede49bcaff4e7a6519ba67c
出典メモuspto-grants-2009_08