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HRID 129691생성일: 2026년 10월 24일

Ethyl Acetate → N-methyl-N-phenethyl-2-(4-benzyloxy-3-formylindol-1-yl)acetamide

https://huagongshe.com/ko/reaction/129691

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물4-(benzyloxy)-1H-indole-3-carbaldehydeHCID 7015846—
반응물N-methyl-N-phenethyl-2-bromoacetamideHCID 10753531—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물N-methyl-N-phenethyl-2-(4-benzyloxy-3-formylindol-1-yl)acetamideHCID 10741107—

반응 단계

To a suspension of sodium hydride (1.31 g, 80% suspension in mineral oil, 43.8 mM) in 65 ml of tetrahydrofuran (THF), cooled in an ice bath, is added dropwise a solution of 4-benzyloxyindole-3-carboxaldehyde (10.2 g, 39.8 mM) in 55 ml of THF. The mixture is stirred in the cooling bath for an additional 30 minutes; N-methyl-N-phenethyl-2-bromoacetamide (15.3 g, 59.7 mM) is then added. The resulting mixture is stirred at room temperature for 18 hours. Ethyl acetate and 50% brine is added and the layers are separated. The organic layer is washed with brine, dried over magnesium sulfate and concentrated in vacuo to give crude product as a beige oil. Purification on preparative HPLC (silica gel column, 20% ethyl acetate in methylene chloride) gives N-methyl-N-phenethyl-2-(4-benzyloxy-3-formylindol-1-yl)acetamide. (m.p. 120°-122° C.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468898
출처 데이터셋uspto-grants-1995_11
ORD IDord-3406eb353d184e8a859d8f4cfef8029d
출처 메모uspto-grants-1995_11