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HRID 82956作成日:2026年10月26日

N-Hydroxyphthalimide → 2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/82956

反応式

関与物質

役割名称HCID仕込み量
反応物N-HydroxyphthalimideHCID 10665—
反応物TriphenylphosphineHCID 11776—
反応物1-(Diphenylmethyl)azetidin-3-olHCID 330448—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒TetrahydrofuranHCID 8028—
生成物2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dioneHCID 6833802437.3%

反応条件

温度0 °C

反応手順

To a solution of N-benzhydrylazetidin-3-ol (1.0 g, 4.18 mmol) in anhydrous THF (66 mL) under nitrogen were added N-hydroxyphthalimide (750 mg, 4.60 mmol) and triphenylphosphine (2.19 g, 8.36 mmol). The reaction mixture was cooled to 0° C. and DEAD (1.52 mL, 8.36 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced. The residue was purified on column chromatography (eluent: pentane/EtOAc 7/3 to 4/6) to give the title compound (600 mg, 37%) as a wax.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846711B2
出典データセットuspto-grants-2014_09
ORD IDord-8db0c46b33d045a3bf08d5ac027168f0
出典メモuspto-grants-2014_09