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HRID 2097114作成日:2026年10月25日

Methylamine → (3-Chloro-benzofuran-2-ylmethyl)methylamine

https://huagongshe.com/reaction/2097114

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物Sodium borohydrideHCID 4311764—
反応物3-Chlorobenzofuran-2-carboxaldehydeHCID 4737020—
溶媒MethanolHCID 887—
生成物(3-Chloro-benzofuran-2-ylmethyl)methylamineHCID 5927758782.1%

反応手順

To a solution of 3-chlorobenzofuran-2-carboxaldehyde (1.62 g, 8.9 mmol) in methanol (50 mL) is added N-methylamine (33% solution in ethanol, 1.11 g, 35.9 mmol) and stirred overnight at room temperature. The mixture is concentrated in vacuo, re-solvated in methanol (50 mL) and cooled in an ice bath. Sodium borohydride (407 mg, 10.8 mmol) is added in portions and the mixture stirred at room temperature for 4 h. The mixture is concentrated in vacuo, re-solvated in 1.3M sodium hydroxide solution, stirred for 20 min, extracted with ethyl acetate, dried with sodium sulfate and concentrated. Purification by column chromatography (silica, CH2Cl2/MeOH, 9/1) gave title compound (1.43 g, 82%) as a colorless oil. 1H NMR (300 MHz, DMSO-d6) δ 7.55-7.63 (m, 2H), 7.33-7.42 (m, 2H), 3.93 (s, 2H), 2.27 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08450307B2
出典データセットuspto-grants-2013_05
ORD IDord-71edb359272c4abe834da01637e39e37
出典メモuspto-grants-2013_05