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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895314Generated: October 30, 2026

Acetic Anhydride → HCID 21872395, compound

https://huagongshe.com/reaction/895314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 12193781HCID 12193781—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
ProductHCID 21872395HCID 2187239592%

Reaction Steps

At 20 to 30° C., 2.56 g of acetic anhydride was added to a mixture of 5.00 g of N-(2-hydroxyethyl)bis[2-(methoxycarbonyl)ethyl]amine, 2.97 g of triethylamine, 50 mg of 4-dimethylaminopyridine and 25 g of THF. The resulting mixture was stirred for 5 hours. Water was added to terminate the reaction. The reaction mixture was then extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the residue was purified by distillation under reduced pressure, whereby 5.30 g of N-(2-acetoxyethyl)bis[2-(methoxycarbonyl)ethyl]amine was obtained (boiling point: 120° C./15 Pa, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916593B2
Source datasetuspto-grants-2005_07
ORD IDord-9f7b83b45e32450b84350119009beff6
Source noteuspto-grants-2005_07