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HRID 661963Erstellt: 24. Oktober 2026

Phenol → 8-Phenoxy-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/de/reaction/661963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt1,4-Dioxaspiro(4.5)decan-8-olHCID 567352—
LösungsmittelDichloromethaneHCID 6344—
Produkt8-Phenoxy-1,4-dioxaspiro[4.5]decaneHCID 1898042332%

Reaktionsschritte

Step 1 A solution of 1,4-dioxaspiro[4.5]decan-8-ol (1.00 g, 6.32 mmol), phenol (0.714 g, 7.59 mmol) and triphenylphosphine (1.824 g, 6.95 mmol) in DCM (21.07 mL) was treated with diisopropyl azodicarboxylate (1.48 mL, 7.59 mmol) and the mixture was stirred at rt for 5 days. The mixture was concentrated and the residue was purified by column chromatography, eluting with a gradient from hexane to 80:20 hexane-EtOAc). The crude product was dissolved in EtOAc and the solution was washed twice with 1 M aqueous sodium hydroxide and brine, dried and concentrated to provide 8-phenoxy-1,4-dioxaspiro[4.5]decane as a colorless liquid (0.468 g, 32%). 1H NMR (500 MHz, chloroform-d) δ 7.16-7.24 (2H, m), 6.81-6.89 (3H, m), 4.30-4.38 (1H, m), 3.85-3.93 (4H, m), 1.80-1.90 (6H, m), 1.50-1.59 (2H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084620B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-7c3e76a7c3c64a4fb31163df383f1410
Quellennotizuspto-grants-2011_12