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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434646Generated: October 30, 2026

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

https://huagongshe.com/reaction/1434646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzylamineHCID 7669—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Octanol, 8-bromo-HCID 162607—
SolventAcetonitrileHCID 6342—
Product8-(N-Benzyl-N-methylamino)octan-1-olHCID 16662153100%

Reaction Conditions

Temperature35 °C

Reaction Steps

8-Bromo-1-octanol (25 g, 119.6 mmol) in acetonitrile (50 mL) was added to a stirred solution of N-benzyl-N-methylamine (43.49 g, 358.9 mmol) and potassium carbonate (49.52 g, 358.9 mmol) in acetonitrile (250 mL) at 35° C. The reaction mixture was then stirred at 35° C. for 7 h and then cooled to ambient temperature. The potassium carbonate was filtered and the filtrate was concentrated under reduced pressure. The crude residue was dissolved in MTBE (400 mL) and the organic phase was washed with water, brine and dried over magnesium sulfate. N-methyl-2-pyrrolidone was added and the mixture was concentrated under reduced pressure to remove excess N-benzyl-N-methylamine. MTBE (400 mL) was added and the organic phase was washed with water, brine, and dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford the title intermediate as an oil (˜100% conversion).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615566B2
Source datasetuspto-grants-2009_11
ORD IDord-b32fe567ff904d259787460e34ec9b4a
Source noteuspto-grants-2009_11