HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369992Generated: October 29, 2026
Diethyl 2-(2-(benzyloxy)ethyl)malonate → 2-[2-(Benzyloxy)ethyl]propane-1,3-diol
https://huagongshe.com/reaction/1369992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl 2-(2-(benzyloxy)ethyl)malonate | HCID 12549951 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[2-(Benzyloxy)ethyl]propane-1,3-diol | HCID 10512639 | 87.4% |
Reaction Steps
To a cooled, stirred suspension of lithium aluminium hydride (103 g, 2.7 mol) in dry ether (2.51) under nitrogen was added ethyl 4-benzyloxy-2-ethoxycarbonyl-butanoate (362 g, 1.23 mol) over a period of 3 hours. On completion of the addition, the reaction mixture was allowed to warm to room temperature, and then heated under reflux for 1 hour. It was then re-cooled and the excess lithium aluminium hydride destroyed by dropwise addition of water (100 ml), 2M sodium hydroxide (100 ml) and water (300 ml). The reaction mixture was filtered, and the filter cake washed well with chloroform. The filtrate was dried (MgSO4), filtered, and evaporated to give 4-benzyloxy-2-hydroxymethylbutan-1-ol as a clear oil (226 g, 87%). δH (CDCl3) 1.35-2.05 (3H, m, CHCH2CH2), 3.30-3.80 (8H, m, 3×CH2O, 2×OH), 4.42 (2H, s, OCH2Ph) 7.26 (5H, s, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579981B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-a2ae02bc8b4a4b508e97d90a179d70f4 |
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| Source note | uspto-grants-2003_06 |
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