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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461510Generated: November 2, 2026

Diethyl 2-(2-(benzyloxy)ethyl)malonate → 2-[2-(Benzyloxy)ethyl]propane-1,3-diol

https://huagongshe.com/reaction/1461510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl 2-(2-(benzyloxy)ethyl)malonateHCID 12549951—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product2-[2-(Benzyloxy)ethyl]propane-1,3-diolHCID 1051263987.4%

Reaction Steps

To a cooled, stirred suspension of lithium aluminum 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), 2 M 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 (3 H, m, CHCH2CH2), 3.30-3.80 (8 H, m, 3×CH2O, 2×OH), 4.42 (2 H, s, OCH2Ph), 7.26 (5 H, s, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075445
Source datasetuspto-grants-1991_12
ORD IDord-5ee7d3a65562493abd0bd377d1694e2b
Source noteuspto-grants-1991_12