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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395888Erstellt: 25. Oktober 2026

8-Oxabicyclo[3.2.1]oct-6-en-3-one → HCID 178456493, Verbindung

https://huagongshe.com/reaction/395888

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-Oxabicyclo[3.2.1]oct-6-en-3-oneHCID 557672—
Edukt8-(8-Hydroxy-8-methyl-bicyclo[3.2.1]oct-3-yl)-1,3-dipropyl-3,7-dihydro-purine-2,6-dioneHCID 18173101—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178456493HCID 178456493—

Reaktionsschritte

To a stirred solution of 1,3-dipropyl-7-pyrrolidin-1-ylmethyl-3,7-dihydro-purine-2,6-dione (Example 48) (522 mg, 1.63 mmol) in THF (50 ml) at −78° C. was added n-BuLi (1.55 M in hexanes, 1.2 eq, 1.3 ml). The color of the resulting yellow mixture deepened to orange-red and was stirred at this temperature for 0.5 h. A solution of 8-oxa-bicyclo[3.2.1]oct-6-en-3-one (1.1 eq, 222 mg, 1.79 mmol) in THF (4 ml) was added via syringe over a period of 20 minutes. The mixture was held at −78° C. for 2 h and allowed to reach ambient temperature overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (20 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting orange oil was purified by chromatography on silica using 5% MeOH in CH2Cl2 as eluent to give a clear oil that solidified upon standing (50 mg, 8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605600B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-2f7ed1c428dc4bc2831aeccb59e669aa
Quellennotizuspto-grants-2003_08