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HRID 12022作成日:2026年10月27日

4-Toluenesulfonyl chloride → 2-Tert-butyl-6-chlorocyclohexanone

https://huagongshe.com/reaction/12022

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物DiisopropylamineHCID 7912—
反応物2-tert-ButylcyclohexanoneHCID 102681—
溶媒TetrahydrofuranHCID 8028—
生成物2-Tert-butyl-6-chlorocyclohexanoneHCID 6868097281%

反応条件

温度-78 °C

反応手順

N-butyl lithium is added dropwise to a solution, cooled to 0° C., of diisopropylamine (5.5 mmol) in dry tetrahydrofuran. After the addition is complete the mixture is cooled to −78° C., and a solution of 2-tert-butylcyclohexanone (5 mmol) in dry tetrahydrofuran (50 ml) is introduced, followed by the addition of p-toluenesulphonyl chloride (5 mmol), also dissolved in dry tetrahydrofuran (50 ml). The reaction mixture is heated to room temperature and after stirring for 30 mins over silica gel filtered with ether as eluant. After concentration by evaporation in a vacuum 2-tert-butyl-6-chlorcyclohexanone (760 mg) is obtained in a yield of 81% (Tet. Lett. 1999, 40(12), 2231-2234).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727979B2
出典データセットuspto-grants-2010_06
ORD IDord-2490bc6217a344258faf2fe00e97dd10
出典メモuspto-grants-2010_06