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HRID 40479作成日:2026年10月24日

Toluene → 2-(5-Bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione

https://huagongshe.com/ja/reaction/40479

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物1,3-CyclopentanedioneHCID 77466—
反応物HCID 178419342HCID 178419342—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Hydrochloric AcidHCID 313—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物2-(5-Bromo-2-cyclopropylphenyl)cyclopentane-1,3-dioneHCID 66676860—

反応条件

温度80 °C

反応手順

To a solution of cyclopentane-1,3-dione (0.57 g, 0.0058 mol) and 4-dimethylaminopyridine (3.64 g, 0.030 mol) in chloroform (33 ml) is added toluene (9 ml) then 5-bromo-2-cyclopropylphenyl lead triacetate (3.77 g, 0.0065 mol). This solution is heated at 80° C. for 20 hours then cooled to room temperature and diluted with dichloromethane and 2M aqueous hydrochloric acid. The resulting biphasic suspension is filtered through diatomaceous earth and the two phases are separated. The organic layer is further washed with 2M aqueous hydrochloric acid and the aqueous phase is extracted again with dichloromethane. All organic fractions are combined, washed with brine, dried over magnesium sulfate then concentrated in vacuo. The crude product is finally purified by flash column chromatography on silica gel (isohexane/ethyl acetate eluant) to afford 2-(5-bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530388B2
出典データセットuspto-grants-2013_09
ORD IDord-34572c46811e4ecc907e60bca4b397f0
出典メモuspto-grants-2013_09