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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6435Erstellt: 23. Oktober 2026

Phenol → (2,2-Diethoxyethoxy)benzene

https://huagongshe.com/de/reaction/6435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktSodium hydrideHCID 24758—
EduktEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Lösungsmittel2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Produkt(2,2-Diethoxyethoxy)benzeneHCID 96328—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Sodium hydride (5.83 g of a 55% dispersion in mineral oil) was added to a solution of phenol (12.56 g) in DMPU (25 ml) at 5° C. and the mixture was stirred for 30 minutes. Bromoacetaldehyde diethyl acetal (10.05 ml) was added and the mixture was heated at 110° C. for 5 hours, then allowed to cool. The mixture was partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic phase was separated and washed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml). The aqueous fractions were combined and re-extracted with ethyl acetate (100 ml). The combined organic extracts were dried (MgSO4) and concentrated. The resultant oil was purified by flash column chromatography, eluting with ethyl acetate/hexane (1:10 v/v) to give 2-phenoxyacetaldehyde diethyl acetal (9.43 g) as an oil; NMR: 1.25(6H,t, J=7.0 Hz), 3.6-3.85(4H,m), 4.05(2 H,d, J=6.0 Hz), 4.85 (1H,t, J=6.0 Hz) and 6.9-7.35(5H,m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05248780
Quelldatensatzuspto-grants-1993_09
ORD IDord-db8a01301d8543ea840e78a021d649d8
Quellennotizuspto-grants-1993_09