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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397162Erstellt: 23. Oktober 2026

1,4-Dioxaspiro[4.5]decan-8-one → 8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/de/reaction/397162

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Edukt(4-Fluorobenzyl)triphenylphosphonium chlorideHCID 2733554—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decaneHCID 1213395079,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirring solution of 4-fluorophenylmethyl triphenylphosphonium chloride (39 g, 96 mmol, Lancaster) in 500 mL of dry THF at −78° C. was added 1 M potassium t-butoxide in THF (106 mL, 106 mmol, Aldrich). The reaction was stirred for 30 min and then warmed to 0° C. The reaction was stirred for 30 min and then 1,4-cyclohexanedione mono-ethylene ketal (15.0 g, 96 mmol, Aldrich) was added. After 30 min, the reaction was warmed to room temperature and allowed to stir overnight. The reaction was heated to reflux for 4 h and then cooled to room temperature. The reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL). The organic layer was separated, washed with brine, dried over sodium sulfate, and conc in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate) to yield 18.9 g of a colorless oil. MS (ESI) 251 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06608227B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-157c8a3c8a5045bd96f3c3605b092e44
Quellennotizuspto-grants-2003_08