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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 650811생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/650811

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물MethanolHCID 887—
반응물Sodium borohydrideHCID 4311764—
반응물3-PhenylpropylformamideHCID 12147094—
용매TetrahydrofuranHCID 8028—
생성물N-Methyl-3-phenylpropan-1-amineHCID 3541753%

반응 조건

온도7 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06274584B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-2b95b98d15cd46cfa6b107d261dde89f
출처 메모uspto-grants-2001_08