HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608216Generated: November 3, 2026
Water → 2-(4-Benzylmorpholin-2-yl)ethan-1-ol
https://huagongshe.com/reaction/1608216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl (4-benzylmorpholin-2-yl)acetate | HCID 12582571 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Benzylmorpholin-2-yl)ethan-1-ol | HCID 14652591 | 99.8% |
Reaction Steps
A solution of 2-ethoxycarbonylmethyl-4-benzylmorpholine (41 g) in diethyl ether (100 ml) is added dropwise to a stirred suspension of lithium aluminum hydride (59.2 g) in diethyl ether (150 ml). The reaction mixture is stirred at 25° C. for 1 hour. The excess of lithium aluminum hydride is decomposed by the successive addition of ethyl acetate and water. The insoluble materials are filtered off, and the filtrate is evaporated to give the title compound (34.4 g) as an oil. The starting material, 2-ethoxycarbonylmethyl-4-benzylmorpholine, is prepared according to the method of F. Loftus [Syn. Commun., 10, 59-73 (1980)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04870074 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-38c5b70e8f36445eab66d2f41d246acf |
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| Source note | uspto-grants-1989_09 |
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