HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071889Generated: November 1, 2026
Methanol → 4-(2-Hydroxyethyl)morpholine-2,3-dione
https://huagongshe.com/reaction/1071889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(2-Hydroxyethyl)morpholine-2,3-dione | HCID 458488 | — |
Reaction Steps
A 4(2-hydroxyethyl)morpholine-2,3-dione was prepared at low temperatures by the following procedure. Into a five-necked 22 liter round bottomed flask equipped with a reflux condenser, nitrogen bubbler, addition funnel, thermocouple well, and mechanical stirrer was charged 3000 g (20.53 mol) of diethyl oxalate and 2000 ml of isopropyl alcohol. The solution was cooled to 0 to 5° C. using a cold bath of ice and methanol. A solution of 2160 g (20.53 mol) of diethanolamine dissolved in 2000 ml of isopropyl alcohol was added through the addition funnel during a period of 5 to 6 hours. The reaction is exothermic. After addition was complete, the mixture was allowed to stand at room temperature overnight. The product is collected by filtration. After air drying, 2923 g (89.5% yield) of white crystals were obtained with identical spectral properties to the compound prepared in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06908539B2 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-1a88f70d0026447cbe7929b604e1e0c2 |
|---|
| Source note | uspto-grants-2005_06 |
|---|