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HRID 650811作成日:2026年10月27日

Iodine → N-Methyl-3-phenylpropan-1-amine

https://huagongshe.com/reaction/650811

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物MethanolHCID 887—
反応物Sodium borohydrideHCID 4311764—
反応物3-PhenylpropylformamideHCID 12147094—
溶媒TetrahydrofuranHCID 8028—
生成物N-Methyl-3-phenylpropan-1-amineHCID 3541753%

反応条件

温度7 °C

反応手順

N-(3-Phenylpropyl)formamide (5.70 g, 34.9 mmol) was dissolved in tetrahydrofuran (50 ml) and added dropwise to a suspension of sodium borohydride (1.58 g, 41.91 mmol) in tetrahydrofuran (100 ml), which was cooled to 7° C. A solution of iodine (4.42 g, 17.46 mmol) in tetrahydrofuran was added dropwise, while the temperature was kept at 7° C. After the addition was finished, the reaction mixture was warmed to reflux for 16 h. The reaction mixture was cooled to 7° C., and methanol (250 ml) was added dropwise. The solvent was removed in vacuo. The residue was dissolved in 20% aqueous sodium hydroxide solution (250 ml) and tert-butyl methyl ether (100 ml). The phases were separated. The aqueous phase was extracted with tert-butyl methyl ether (2×100 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (400 g), using dichicromethane/methanol/25% aqueous ammonia (100:10:1) as eluent to give 2.76 g of N-methyl-N-(3-phenylpropyl)amine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06274584B1
出典データセットuspto-grants-2001_08
ORD IDord-2b95b98d15cd46cfa6b107d261dde89f
出典メモuspto-grants-2001_08