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HRID 226213作成日:2026年10月24日

3-Methoxybenzylamine → HCID 57754052、化合物

https://huagongshe.com/ja/reaction/226213

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethoxybenzylamineHCID 21156—
反応物Ammonium ChlorideHCID 25517—
反応物Trifluoromethanesulfonic acid, lithium saltHCID 3664839—
反応物(1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl esterHCID 86616462—
溶媒AcetonitrileHCID 6342—
生成物HCID 57754052HCID 57754052—

反応手順

A solution of (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester (0.03 g, 0.1 mmol) in acetonitrile (1 mL) was treated with lithium triflate (0.032 g, 0.2 mmol) and stirred at ambient temperature for 20 minutes. Then 3-methoxybenzylamine (0.016 mL, 0.12 mmol) was added to the reaction neat in one portion. The reaction was stirred at ambient temperature for 14 hours. The reaction was poured into saturated ammonium chloride solution (5 mL), extracted with ethyl acetate, the organic phase separated, dried (MgSO4) and the solvent removed at reduced pressure. The product was obtained as an oil and used without further purification (0.041 g, 94%). MS: 437 (M+H, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557137B2
出典データセットuspto-grants-2009_07
ORD IDord-102b0fd138274c048ebe5de232edecef
出典メモuspto-grants-2009_07