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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584384생성일: 2026년 10월 25일

N-Hydroxyphthalimide → 4-Methoxymethoxybenzyloxyamine

https://huagongshe.com/reaction/584384

반응식

참여 물질

역할이름HCID투입량
반응물N-HydroxyphthalimideHCID 10665—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물4-MethoxymethoxybenzylalcoholHCID 11607984—
용매TetrahydrofuranHCID 8028—
생성물4-MethoxymethoxybenzyloxyamineHCID 1105229258%

반응 단계

Diethyl azodicarboxylate (40% toluene solution, 142 g) was added dropwise to a solution of 4-methoxymethoxybenzylalcohol (50.0 g), N-hydroxyphthalimide (44.1 g) and triphenylphosphine (83.7 g) in tetrahydrofuran (900 ml) at room temperature and stirred for 1 hour. The reaction mixture was concentrated. In order to remove triphenylphosphine oxide, the residue was subjected to silica gel chromatography to obtain crystals from an ethyl acetate-hexane (1:5, v/v)-eluted fraction. The crystals were washed with ethyl acetate-hexane (1:5, v/v) and then dissolved in tetrahydrofuran (200 ml) and ethanol (50 ml). To this solution was added hydrazine monohydrate (33.7 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, an aqueous solution of potassium carbonate was added and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. Isopropyl ether was added to the residue and filtered to remove insolubles. The filtrate was concentrated to obtain 4-methoxymethoxybenzyloxyamine (28.9 g, yield 58%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924300B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-055ac7dae779481188ca682c7155401c
출처 메모uspto-grants-2005_08