HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584229Generated: October 26, 2026
Ethanol → (4-Benzyl-3-methylmorpholin-3-yl)methanol
https://huagongshe.com/reaction/584229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Reactant | 4-Benzyl-5-(hydroxymethyl)-5-methylmorpholin-3-one | HCID 22342739 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-Benzyl-3-methylmorpholin-3-yl)methanol | HCID 22342862 | 92.3% |
Reaction Steps
Sodium bis(2-methoxyethoxy)aluminum hydride (3.46 M solution in toluene; 42 ml) was added to a solution of 4-benzyl-5-hydroxymethyl-5-methyl-3-morpholinone (10.77 g) in toluene (100 ml) at 0° C. under nitrogen atmosphere and the whole was stirred at room temperature for 1 hour. Ethanol (20 ml) was added to the mixture at 0° C. and the pH of the mixture was adjusted to 12 by 1N sodium hydroxide solution. The organic layer was separated, added 1N hydrochloric acid and the acidic aqueous layer was separated. This procedure was repeated twice and the combined aqueous layer was made alkaline with 4 M sodium hydroxide solution. It was extracted with ethyl acetate, dried over magnesium sulfate and evaporated in vacuo to give 4-benzyl-3-hydroxymethyl-3-methylmorpholine (9.35 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924278B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-a1e671d68459494080d24db9d0fce367 |
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| Source note | uspto-grants-2005_08 |
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