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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082325Generated: November 2, 2026

Acetylethanolamine → HCID 178474919, compound

https://huagongshe.com/reaction/2082325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylethanolamineHCID 8880—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 178527054HCID 178527054—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178474919HCID 17847491929.7%

Reaction Steps

To a solution of 0.31 g (1.5 mmol) of 1,3-dicyclohexylcarbodiimide in tetrahydrofuran (3 ml) is added 0.28 g (1.5 mmol) of 3-phenylpropylphosphinic acid in tetrahydrofuran (1 ml). The resulting suspension is stirred for 10 minutes at room temperature. N-acetyl ethanolamine (0.10 g, 1.0 mol) is then added, followed by 18 mg or 4-dimethylaminopyridine. The mixture is stirred for 2 hours. The solvent is evaporated under reduced pressure, and the residue is stirred with ethyl acetate (20 ml). The resulting suspension is filtered. The filtrate is washed with 5% potassium hydrogen sulfate (8 ml), saturated sodium bicarbonate (2×5 ml), and brine (5 ml), and evaporated to give 0.12 g of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189023
Source datasetuspto-grants-1993_02
ORD IDord-e097ebdedb164acfaf46a0b775e3c606
Source noteuspto-grants-1993_02