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HRID 250490作成日:2026年10月27日

Hydrochloric Acid → 5-Cyclohexylsulfanyl-isoindole-1,3-dione

https://huagongshe.com/reaction/250490

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-NitrophthalimideHCID 6969—
反応物Potassium CarbonateHCID 11430—
反応物CyclohexanethiolHCID 15290—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物5-Cyclohexylsulfanyl-isoindole-1,3-dioneHCID 66712998114.7%

反応手順

A mixture of 5-nitro-isoindole-1,3-dione (10.0 g), cyclohexanethiol (9.1 g) and potassium carbonate (18.7 g) in acetone (260 ml) was heated to reflux overnight. After cooling, the mixture was diluted with water (250 ml) and then acidified by 6 N HCl to pH=4. Precipitate was collected and dried in vacuo to give the intermediate 5-cyclohexylsulfanyl-isoindole-1,3-dione (15.6 g). This intermediate was dissolved in acetone (170 ml) and to the mixture was added bromo ethylacetate (10.6 g) and potassium carbonate (23.8 g). The mixture was refluxed overnight. After cooling, reaction mixture was filtered and rinsed with ethyl acetate. Filtrate was concentrated and purified by silica gel chromatography (10%-50% ethyl acetate in methylene chloride) to give the title compound (13.1 g). 1H NMR (200 MHz, CDCl3) δ 7.73 (m, 2H), 7.56 (dd, J=7.8, 1.6 Hz, 1H), 4.40 (s, 2H), 4.21 (q, J=7.0 Hz, 2H), 3.37 (m, 1H), 2.07-1.28 (m, 13H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863292B2
出典データセットuspto-grants-2011_01
ORD IDord-8ac5c61566df40678a244d34121bd897
出典メモuspto-grants-2011_01