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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727304Generated: October 25, 2026

Diethyl Ether → 3-((Benzyloxy)methyl)cyclobutanone

https://huagongshe.com/reaction/1727304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant3-(Benzyloxymethyl)-2,2-dichlorocyclobutanoneHCID 10355186—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product3-((Benzyloxy)methyl)cyclobutanoneHCID 11819850—

Reaction Conditions

Temperature60 °C

Reaction Steps

Zinc dust (93.5 g, 1.44 mol) was added to a solution of 3-(benzyloxymethyl)-2,2-dichlorocyclobutanone (124 g, 0.48 mol) in glacial acetic acid (800 ml) at room temperature. The reactants were heated at 60° C. for 1 hr, after which time dry diethyl ether was added to the cooled products, which were then filtered. The residue was washed with diethyl ether and the combined filtrate and washings were concentrated under reduced pressure. The residue was dissolved in dichloromethane, which was washed with saturated NaHCO3 twice and water once. The organic phase was dried over MgSO4 and the solvent was evaporated to give an oily product, which was purified by column chromatography (Hexane:EtOAc=6:1). 1H NMR (CDCl3, 400 MHz): δ 2.70 (m, 1H), 2.84-2.92 (m, 2H), 3.08-3.18 (m, 2H), 3.59 (d, J=6.4, 2H), 4.56 (s, 2H), 7.28-7.38 (m, 5H). 13C NMR (CDCl3, 100 MHz): δ 23.88, 50.26, 73.11, 73.42, 127.88, 127.99, 128.68, 138.26, 207.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495006B2
Source datasetuspto-grants-2009_02
ORD IDord-f3009f36b5074d57a6c22dfb2f4b640e
Source noteuspto-grants-2009_02