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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1727304Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1727304

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt3-(Benzyloxymethyl)-2,2-dichlorocyclobutanoneHCID 10355186—
KatalysatorZincHCID 23994—
LösungsmittelAcetic AcidHCID 176—
Produkt3-((Benzyloxy)methyl)cyclobutanoneHCID 11819850—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07495006B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-f3009f36b5074d57a6c22dfb2f4b640e
Quellennotizuspto-grants-2009_02