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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241307Generated: October 26, 2026

Maleic Acid → (R)-2-hydroxymethylmorpholine maleate

https://huagongshe.com/reaction/241307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
ReactantMorpholin-2-ylmethanolHCID 3497988—
Reactant1,4-OxazepaneHCID 21873275—
SolventMethanolHCID 887—
Product(R)-2-hydroxymethylmorpholine maleateHCID 6666303839.2%

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648190B2
Source datasetuspto-grants-2014_02
ORD IDord-13884569a82c4024a5c7ecfe0ac15eed
Source noteuspto-grants-2014_02