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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514631Generated: October 30, 2026

Hydrochloric Acid → Diethyl 2-(2-(benzyloxy)ethyl)malonate

https://huagongshe.com/reaction/514631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 2-(2-(benzyloxy)ethyl)malonateHCID 1254995190.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

506 mg (60% in oil, 13 mmol equivalents) of sodium hydride was added to 5.0 mL of tetrahydrofuran, and the mixture was cooled to about 0° C. in an ice bath. 3.2 mL (20.7 mmol equivalents) of diethyl malonate was added thereto (solution A). 2.3 g (10.7 mmol equivalents) of 2-benzyloxy-1-bromoethane was dissolved in 3.0 mL of tetrahydrofuran, this was added dropwise to solution A over 10 minutes, and the mixture was refluxed while heating overnight. After completion of the reaction, a 0.5 mol/L aqueous solution of hydrochloric acid was added dropwise to the reaction liquid, and the mixture was extracted three times with diethyl ether. The combined diethyl ether layers were washed with brine, then dried with anhydrous magnesium sulfate, and subsequently concentrated under vacuum, and the obtained crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (v/v)=20/1) to give 2.85 g (9.67 mmol equivalents) of diethyl 2-(2-benzyloxyethyl)malonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107964B2
Source datasetuspto-grants-2015_08
ORD IDord-16621d2bbf0e4bb493233f7fb6ea4bc1
Source noteuspto-grants-2015_08