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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906228Generated: November 2, 2026

Ethoxalyl chloride → HCID 44902124, compound

https://huagongshe.com/reaction/906228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantDiisopropylethylamineHCID 81531—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 44902124HCID 4490212435.1%

Reaction Steps

To a mixture of (4-methoxyphenyl)methanamine (9.90 g, 72.2 mmol) in THF (40 mL) was slowly added ethyl 2-chloro-2-oxoacetate (10.84 g, 79 mmol). After stirring the reaction at RT for 15 min, a solution of 2,2-dimethoxyethanamine (9.10 g, 87 mmol) and N,N-diisopropylethylamine (37.8 mL, 217 mmol) in EtOAc (40.0 mL) was added. The reaction was heated at reflux for 18 hours; whereupon, after cooling to RT, saturated NaHCO3 (50 ml) was added and the mixture extracted with EtOAc (50 ml). The EtOAc layer was dried over Na2SO4 and concentrated. The crude product was purified by silica gel chromatography employing a solvent gradient (CH2Cl2 to 5% MeOH/CH2Cl2) to elute N1-(2,2-dimethoxyethyl)-N2-(4-methoxybenzyl)oxalamide (7.50 g, 25.3 mmol, 35.1% yield) as white solid. 1H NMR (400 MHz, chloroform-d) δ ppm 9.07 (1H, s), 7.69 (1H, t, J=5.65 Hz), 7.59 (1H, d, J=8.78 Hz), 6.74 (1H, d, J=8.78 Hz), 4.46 (1H, t, J=5.40 Hz), 3.79 (2H, s), 3.53 (2H, t), 3.44 (6H, s), 2.23 (6H, d, J=5.27 Hz), 1.37 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012984B2
Source datasetuspto-grants-2011_09
ORD IDord-e261fc2c47b240589a0d41d18630637d
Source noteuspto-grants-2011_09