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HRID 1021389作成日:2026年10月26日

3-Chlorobenzaldehyde → cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide

https://huagongshe.com/reaction/1021389

反応式

関与物質

役割名称HCID仕込み量
反応物3-ChlorobenzaldehydeHCID 11477—
反応物(3-(1,3-Dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromideHCID 22018487—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimideHCID 5867982682%

反応条件

温度-75 °C

反応手順

To a stirred suspension of (3-(1,3-dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromide (17.6 g, 33.2 mmol) in tetrahydrofuran (170 mL) at ambient temperature was added 3-chlorobenzaldehyde (3.76 mL, 33.2 mmol), and the resulting mixture was cooled with a dry-ice acetone bath to −75° C. Solid potassium t-butoxide (3.72 g, 33.2 mmol) was added, and stirring was continued in the bath for an additional 20 minutes; the temperature was −80° C. The cooling bath was removed, and when the internal temperature reached −30° C., the flask was placed in a water-ice bath. The temperature eventually settled at 10° C. and was maintained for 2 hours. The reaction mixture was poured into a separatory funnel containing water (250 mL), and this was extracted with ethyl acetate (250 mL) The organic layer was dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel, eluting with 90/10 hexanes/ethyl acetate, to afford (Z)-2-(4-(3-chlorophenyl)but-3-enyl)isoindoline-1,3-dione as a white solid (8.46 g, 82% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716498B2
出典データセットuspto-grants-2014_05
ORD IDord-869772aa87af411d9ac61c0755a9ad4c
出典メモuspto-grants-2014_05