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HRID 435729作成日:2026年10月26日

2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dione → Phthalimide

https://huagongshe.com/reaction/435729

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dioneHCID 28777—
溶媒HeptaneHCID 8900—
生成物PhthalimideHCID 6809—

反応手順

13.1 Grams (0.05 mole) of N-(cyclohexylthio)phthalimide and 6.9 grams (0.05 mole) of benzoyl thiol(thiobenzoic acid) in 150 ml of heptane are stirred overnight at room temperature. The precipitate is recovered by filtration, washed with carbon tetrachloride and dried. 7.3 Grams of phthalimide (m.p. 234° C) are obtained. The solvent is removed from the filtrate by evaporation under reduced pressure. 12 Grams (95% yield) of product, a light brown liquid, are obtained. The identity of the benzoylcyclohexyl disulfide is confirmed by GLC and NMR analyses. Analysis gives 25.51% sulfur compared to 25.45% sulfur calculated for C13H16OS2. Similarly, except N-(2-benzothiazolylthio)phthalimide is one reactant, there is obtained benzoyl-2-benzothiazolyl disulfide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04006155
出典データセットuspto-grants-1977_02
ORD IDord-1f3f968f02cf4a27bffac25feb1237a1
出典メモuspto-grants-1977_02