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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638772Generated: October 30, 2026

Ammonia → N,N-Dimethyl-3,4-dioleyloxybenzylamine

https://huagongshe.com/reaction/638772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium borohydrideHCID 4311764—
Reactant3,4-DioleyloxybenzaldehydeHCID 16103016—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
ProductN,N-Dimethyl-3,4-dioleyloxybenzylamineHCID 23642188—

Reaction Steps

To a solution of triethylamineamine (2.0 mL, 14 mmol) in ethanol (20 mL) was added dimethylamine hydrochloride (1.63 g, 20 mmol), titanium tetraisopropoxide (5.96 mL, 20 mmol) and 3,4-dioleyloxybenzaldehyde (6.39 g, 10 mmol). The mixture was allowed to stir under argon for 10 h at room temperature. Sodium borohydride (0.57 g, 15 mmol) was added to the reaction mixture which was then allowed to stir at room temperature overnight. Concentrated aqueous ammonia (4 mL) was added slowly to the reaction mixture. The reaction mixture was filtered and the solids washed with dichloromethane. The filtrate was dried over K2CO3, filtered and concentrated. The resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient) to afford 5.81 g (87-+%) of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691405B2
Source datasetuspto-grants-2010_04
ORD IDord-3ed07e4e92d04d8fa9dd75535ac37a43
Source noteuspto-grants-2010_04