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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113099Generated: October 30, 2026

Phenethylamine → 8-(Benzylmethylamino)octan-1-ol

https://huagongshe.com/reaction/2113099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant1-Octanol, 8-chloro-HCID 90012—
SolventAcetonitrileHCID 6342—
Solventtert-Butyl methyl etherHCID 15413—
Product8-(Benzylmethylamino)octan-1-olHCID 6887863096.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

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 ACN (1000 mL) and the resulting suspension was stirred at 80° C. for 20-30 hours. The reaction mixture was then concentrated to a volume of about 500 mL and water (600 mL) and MTBE (1000 mL) were added. The MTBE layer was then separated and washed with water (500 mL). The MTBE solution was concentrated under vacuum and the resulting 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 numberUS07524880B2
Source datasetuspto-grants-2009_04
ORD IDord-de841d7090514f18a8ab96166ad0a3d5
Source noteuspto-grants-2009_04