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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112433Generated: October 30, 2026

Dimethyl Sulfoxide → N-(3-formylbenzyl)succinamic acid tert-butyl ester

https://huagongshe.com/reaction/2112433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(3-(hydroxymethyl)benzyl)succinamic acid tert-butyl esterHCID 57642058—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-(3-formylbenzyl)succinamic acid tert-butyl esterHCID 5764204769.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

At −78° C., oxalyl chloride (0.142 ml, 1.63 mmol) was added dropwise to a solution of dimethyl sulphoxide (0.232 ml. 3.26 mmol) in dichloromethane (5 ml). The reaction mixture was stirred for 10 min at −78° C. A solution of N-(3-(hydroxymethyl)benzyl)succinamic acid tert-butyl ester (372 mg, 1.55 mmol) in dichloromethane (5 ml) was added. The reaction mixture was stirred at −78° C. for 10 min. Triethylamine (1.08 ml, 7.77 mmol) was added. The reaction mixture was stirred at −78° C. for 5 min and then warmed to room temperature. It was stirred at room temperature for 40 min and diluted with ethyl acetate (100 ml). It was washed with a 10% aqueous solution of sodium hydrogensulphate (100 ml). The aqueous phase was extracted with ethyl acetate (2×50 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (150 ml) and dried over magnesium sulphate. The solvent was removed to give 312 mg of crude N-(3-formylbenzyl)succinamic acid tert-butyl ester, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524813B2
Source datasetuspto-grants-2009_04
ORD IDord-72881dc3276d47b3bbca3fb418ecb9d0
Source noteuspto-grants-2009_04