HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241307Generated: October 26, 2026
Maleic Acid → (R)-2-hydroxymethylmorpholine maleate
https://huagongshe.com/reaction/241307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Morpholin-2-ylmethanol | HCID 3497988 | — |
| Reactant | 1,4-Oxazepane | HCID 21873275 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-2-hydroxymethylmorpholine maleate | HCID 66663038 | 39.2% |
Reaction Steps
To a mixture of 2-hydroxymethylmorpholine and 1,4-oxazepane compound (20.0 g, 2-hydroxymethylmorpholine:1,4-oxazepane compound=75.8:24.2) synthesized in Example 5 were added methanol (100 ml) and maleic acid (17.5 g, 0.151 mol) and the mixture was stirred for 30 min. Methanol was evaporated under reduced pressure. To the residue was added 2-propanol (50 ml) and the mixture was subjected twice to azeotropic distillation with dehydrating. To the residue after azeotropic distillation with dehydrating was added ethyl acetate (100 ml) at 40° C., and the mixture was cooled to 10° C. After crystallization, the mixture was cooled to 0° C. and stirred for 1 hr. The crystals were collected by filtration, washed withed twice with ethyl acetate (25 ml) and dried (1 mmHg, 40° C.) to give (R)-2-hydroxymethylmorpholine maleate (13.8 g) (2-hydroxymethylmorpholine:maleic acid=1:1, yield from (S)-epichlorohydrin: 39.2%). The obtained (R)-2-hydroxymethylmorpholine maleate was analyzed by HPLC to find an optical purity of 99% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648190B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-13884569a82c4024a5c7ecfe0ac15eed |
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| Source note | uspto-grants-2014_02 |
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