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HRID 2172012作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/2172012

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US09051321B2
出典データセットuspto-grants-2015_06
ORD IDord-d0a31ed623b44b9582b5a1c6d06ff3fe
出典メモuspto-grants-2015_06