HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969263Generated: October 29, 2026
Hydrochloric Acid → Ethyl morpholine-3-carboxylate
https://huagongshe.com/reaction/969263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Morpholinecarboxylic acid | HCID 3340152 | — |
| Product | Ethyl morpholine-3-carboxylate | HCID 18354446 | — |
Reaction Steps
A solution of morpholine-3-carboxylic acid (4.035 g; 30.8 mmol) in ethanol (250 ml) was saturated with gaseous HCl, then stirred for a week. The solvent was evaporated and the residue taken up in water and made basic (pH˜10) with sodium hydrogen carbonate and sodium carbonate. The mixture was then extracted with dichloromethane (7×), the combined extracts dried (Na2SO4) and the solvent evaporated to give ethyl morpholine-3-carboxylate (746 mg). EIMS: m/z=160.4 [M+H]+. This ester derivative and lithium aluminium hydride (1 M in THF, 9.4 ml, 9.4 mmol) were carefully combined under a nitrogen atmosphere and following addition were heated to reflux. After 5 h the reaction was cooled to room temperature and carefully quenched using dropwise water addition with ice cooling, then filtered and washed with dichloromethane. The solvent was evaporated to give 3-(hydroxymethyl)morpholine (409 mg). EIMS: m/z=118.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307073B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-f5dff8749ff84db098657cf854940b0e |
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| Source note | uspto-grants-2007_12 |
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