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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650811Generated: October 25, 2026

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

https://huagongshe.com/reaction/650811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant3-PhenylpropylformamideHCID 12147094—
SolventTetrahydrofuranHCID 8028—
ProductN-Methyl-3-phenylpropan-1-amineHCID 3541753%

Reaction Conditions

Temperature7 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274584B1
Source datasetuspto-grants-2001_08
ORD IDord-2b95b98d15cd46cfa6b107d261dde89f
Source noteuspto-grants-2001_08