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HRID 41400作成日:2026年10月26日

P-Toluenesulfonamide → 5-Chloro-2-tosylisoindoline

https://huagongshe.com/reaction/41400

反応式

関与物質

役割名称HCID仕込み量
反応物P-ToluenesulfonamideHCID 6269—
反応物Sodium hydrideHCID 24758—
反応物1,2-Bis(bromomethyl)-4-chlorobenzeneHCID 15008226—
溶媒DimethylformamideHCID 6228—
生成物5-Chloro-2-tosylisoindolineHCID 1516789164.2%

反応手順

To a suspension of 60% sodium hydride (3.0 g, 0.125 mmol) in mineral oil in 80 ml of anhydrous DMF (100 ml) was dropwise added a solution of para-toluene sulphonamide (5.6 g, 32.60 mmol) in 30 ml of DMF over 1 hour with vigorous stirring at room temperature. After the addition, the mixture was stirred for 1 hour at room temperature and another 1 hour heating at 90° C. To this mixture was added dropwise a solution of 1,2-bis-bromomethyl-4-chloro-benzene (4 g, 14.18 mmol) in 20 ml of anhydrous DMF at 60° C. and then stirred overnight at room temperature. The resultant mixture was poured onto ice and the resulting precipitate was collected by filtration. The precipitate was washed with 1N hydrochloric acid, 5% sodium carbonate and brine then dried (MgSO4), filtered and evaporated to give 2.8 g of 5-Chloro-2-(toluene-4-sulphonyl)-2,3-dihydro-1H-isoindole as a pale yellow solid. MS: [M+H]+ 308

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530469B2
出典データセットuspto-grants-2013_09
ORD IDord-e46a8b15d74247f19833f1cb90d740fc
出典メモuspto-grants-2013_09