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HRID 72257作成日:2026年10月26日

Toluene → 3-(5-Chloro-2-methylphenyl)bicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/72257

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Bicyclo(3.2.1)octane-2,4-dioneHCID 144686—
反応物[Diacetyloxy-(5-chloro-2-methylphenyl)plumbyl] acetateHCID 178476526—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒ChloroformHCID 6212—
生成物3-(5-Chloro-2-methylphenyl)bicyclo[3.2.1]octane-2,4-dioneHCID 6848551733.3%

反応手順

To a solution of 5-chloro-2-methylphenyllead triacetate (0.41 g, 0.80 mmol) in chloroform (4 ml) is added bicyclo[3.2.1]octane-2,4-dione (0.10 g, 0.72 mmol) and 4-dimethylaminopyridine (0.46 g, 3.62 mmol), and the reaction mixture is stirred at room temperature for 5 minutes. Next toluene (1 ml) is added, and the mixture is stirred at 80° C. for 1 hour (pre-heated oil bath). The reaction mixture is allowed to cool to room temperature, quenched with 1M hydrochloric acid, and the organic phase separated. The aqueous phase is further washed with dichloromethane (×2), and again the phases are separated. All organics are combined then evaporated under reduced pressure to give a crude oil. Purification by preparative reverse-phase HPLC furnishes 3-(5-chloro-2-methylphenyl)bicyclo[3.2.1]octane-2,4-dione (0.063 g, 33%) as a colourless gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828908B2
出典データセットuspto-grants-2014_09
ORD IDord-52e14d12fcc5455ea0366d1449ee46b8
出典メモuspto-grants-2014_09