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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 650811Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/650811

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktMethanolHCID 887—
EduktSodium borohydrideHCID 4311764—
Edukt3-PhenylpropylformamideHCID 12147094—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-Methyl-3-phenylpropan-1-amineHCID 3541753%

Reaktionsbedingungen

Temperatur7 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06274584B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-2b95b98d15cd46cfa6b107d261dde89f
Quellennotizuspto-grants-2001_08