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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367798Generated: November 1, 2026

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

https://huagongshe.com/reaction/1367798

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 numberUS07893302B2
Source datasetuspto-grants-2011_02
ORD IDord-8721436c21904e9a8aad66f982846e20
Source noteuspto-grants-2011_02