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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2172012생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물N-HydroxyphthalimideHCID 10665—
반응물TriphenylphosphineHCID 11776—
반응물1-(Diphenylmethyl)azetidin-3-olHCID 330448—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dioneHCID 6833802437.3%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09051321B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-d0a31ed623b44b9582b5a1c6d06ff3fe
출처 메모uspto-grants-2015_06