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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 265350Erstellt: 25. Oktober 2026

Ammonium Chloride → HCID 54211786, Verbindung

https://huagongshe.com/reaction/265350

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt5-Phenyl-1-pentyneHCID 74573—
Edukt6-Methoxy-1-oxaspiro[2.5]oct-5-en-4-oneHCID 19034373—
EduktButyllithiumHCID 178418339—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 54211786HCID 54211786103,7%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

74 ml (0.118 mol) of n-butyllithium (1.6 molar in hexane) are added dropwise, under a nitrogen atmosphere, to a solution, cooled to -78° C., of 25 ml (0.157 mol) of 5-phenylpentyne in 400 ml of anhydrous diethyl ether. The whole is stirred at -78° C. for 15 minutes and then at 0° C. for 75 minutes. There is then added dropwise to that solution a solution, cooled to -78° C., of 6-methoxy-1-oxa-spiro[2.5]oct-5-en-4-one (11 g; 71.33 mmol) in 80 ml of anhydrous toluene. After 1 hour's stirring at -78° C., the reaction mixture is poured into an aqueous 10% ammonium chloride solution (1000 ml). Conventional treatment of the organic phase yields 22 g (74 mmol) of 4-hydroxy-6-methoxy-4-(5-phenylpenten-1-yl)-1-oxa-spiro[2.5]octene (2 isomers) in the form of an oily residue which is used in the following step without being purified. Hydrogenation of a solution of 22 g (74 mmol) of that mixture of isomers in 610 ml of benzene in the presence of 10 g of Lindlar catalyst for a period of 7 hours results, after filtration and evaporation, in 22 g (73 mmol) of 4-hydroxy-6methoxy-4-(5-phenylpentyl)-1-oxa-spiro[2.5]oct-5-ene in the form of an oily residue which is used in the following step without being purified.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05648382
Quelldatensatzuspto-grants-1997_07
ORD IDord-f305ffeb72e345eb8bc4620c15cd39fc
Quellennotizuspto-grants-1997_07