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HRID 129691作成日:2026年10月26日

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

https://huagongshe.com/reaction/129691

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium hydrideHCID 24758—
反応物4-(benzyloxy)-1H-indole-3-carbaldehydeHCID 7015846—
反応物N-methyl-N-phenethyl-2-bromoacetamideHCID 10753531—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物N-methyl-N-phenethyl-2-(4-benzyloxy-3-formylindol-1-yl)acetamideHCID 10741107—

反応手順

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.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468898
出典データセットuspto-grants-1995_11
ORD IDord-3406eb353d184e8a859d8f4cfef8029d
出典メモuspto-grants-1995_11