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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 619321Erstellt: 23. Oktober 2026

Carbon Dioxide → 3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acid

https://huagongshe.com/de/reaction/619321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktHydrochloric AcidHCID 313—
EduktAmmonium ChlorideHCID 25517—
Edukt3-(1-Adamantyl)-4-(t-butyldimethylsilyloxy)bromobenzeneHCID 10788316—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acidHCID 13633559—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

9.3 g of (2-adamantan-1-yl-4-bromo-phenoxy)-tert-butyl-dimethylsilane were dissolved in 120 ml of absolute tetrahydro-furan and treated dropwise at -78° C. with 15.5 ml of a 1.6 molar solution of n-butyl-lithium in hexane. After stirring at -78° C. for 1.5 hours, a vigorous stream of carbon dioxide was introduced for one hour. Subsequently, the reaction mixture was firstly poured into ice-cold, saturated, aqueous ammonium chloride solution, acidified cautiously to pH 3 with cold 2N hydrochloric acid and extracted with ethyl acetate. After washing once with water, drying over sodium sulfate and evaporation there was obtained a white, crystalline mass which was recrystallized from ethyl acetate and gave 7 g of 3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acid. m.p. 250-252° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05958956
Quelldatensatzuspto-grants-1999_09
ORD IDord-368773ed1f4c461dbc131217641165c6
Quellennotizuspto-grants-1999_09