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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925006Generated: October 29, 2026

2-(Dimethylamino)ethanol → 3-[2-(Dimethylamino)ethoxy]-4-methoxybenzaldehyde

https://huagongshe.com/reaction/925006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-[2-(Dimethylamino)ethoxy]-4-methoxybenzaldehydeHCID 2098629031.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(dimethylamino)ethanol (5.0 g, 56.0 mmol) and triethylamine (8.5 g, 84.0 mmol) in anhydrous DCM (50 mL) was added methanesulfonyl chloride (7.1 g, 62.0 mmol) at 0° C. under N2. The mixture was stirred at 0° C. for 1 hour The solvent was removed in vacuo (6.0 g, yield 65%), and the crude was taken up in CH3CN (100 mL). 3-hydroxy-4-methoxybenzaldehyde (5.5 g, 36.0 mmol) and potassium carbonate (13.8 g, 100.0 mol) was added and reaction was refluxed under N2 overnight. An aqueous/EtOAc workup was followed, and crude was purified by silica gel column chromatography (PE: EtOAc=3:1) to give product (2.5 g, yield 31%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283229B2
Source datasetuspto-grants-2016_03
ORD IDord-6c4525fc221844d8b8d97a869c326ebb
Source noteuspto-grants-2016_03