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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898172Generated: October 26, 2026

Phenethylamine → 8-(N-Benzyl-N-methylamino)octan-1-ol

https://huagongshe.com/reaction/898172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
Reactant1-Octanol, 8-chloro-HCID 90012—
Solventtert-Butyl methyl etherHCID 15413—
Product8-(N-Benzyl-N-methylamino)octan-1-olHCID 1666215396%

Reaction Conditions

Temperature80 °C

Reaction Steps

From 8-Chlorooctan-1-ol: A 2-L flask was charged with benzylmethylamine (270 g, 2.23 mol), sodium carbonate (157 g, 1.48 mol), sodium iodide (11.1 g, 0.074 mol), 8-chlorooctanol (122 g, 0.74 mol) and acetonitrile (1000 mL) and the resulting suspension was stirred at 80° C. for 20-30 h. The reaction mixture was then concentrated to a volume of about 500 mL and water (600 mL) and tert-butyl methyl ether (1000 mL) were added. The MTBE layer was then separated and washed with water (500 mL). The MTBE solution was concentrated by distillation under vacuum to provide an oil and the oil was then further concentrated by distillation under high vacuum to remove excess benzylmethylamine. N-methyl-2-pyrrolidone (300 mL) was then added to the remaining oil and this solution concentrated by distillation under high vacuum to provide an oil. The oil was dissolved in MTBE (1000 mL) and the resulting solution was washed with water (2×500 mL), brine (500 mL), dried with sodium sulfate (100 g), filtered and concentrated by distillation to afford the title compound as an oil (178 g, 96% yield, >95% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351717B2
Source datasetuspto-grants-2008_04
ORD IDord-db32a0c1d1154ee98a508be9e48fff25
Source noteuspto-grants-2008_04