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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669350Generated: October 26, 2026

Dimethyl Sulfoxide → 3-[(2-Methoxyethoxy)carbonylamino]benzaldehyde

https://huagongshe.com/reaction/1669350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67347770HCID 67347770—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-[(2-Methoxyethoxy)carbonylamino]benzaldehydeHCID 2313180658.6%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a mixture of 13 ml of oxalyl chloride and 400 ml of dichloromethane was added dropwise a solution of 23 ml of dimethyl sulfoxide in 40 ml of dichloromethane at −60° C. for 15 minutes. After stirred at −60° C. for 10 minutes, a solution of 30.2 g of 3-[(2-methoxyethoxy)carbonylamino]benzyl alcohol in 100 ml of dichloromethane was added dropwise at −60° C. for 25 minutes. After stirred at −60° C. for 20 minutes, 56 ml of triethylamine was added dropwise at −60° C. for 15 minutes. After stirred at room temperature for 45 minutes, water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed successively with water and then an aqueous saturated sodium chloride solution. After dried over anhydrous magnesium sulfate and then concentration, the resulting crude crystals were washed with t-butyl methyl ether and then dried to obtain 17.55 g of 3-[(2-methoxyethoxy)carbonylamino]benzaldehyde [Compound No. (h)] as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989478B2
Source datasetuspto-grants-2011_08
ORD IDord-f2c9df6d676e43c58c6a2c7ac31d7495
Source noteuspto-grants-2011_08