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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 646042Erstellt: 25. Oktober 2026

Nitric Acid → 2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acid

https://huagongshe.com/reaction/646042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktSulfuric AcidHCID 1118—
Edukt2-(Adamantan-1-yl)-2-bromoacetic acidHCID 2769715—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acidHCID 3274614—

Reaktionsbedingungen

Temperatur28 °C

Reaktionsschritte

α-Bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) is then reacted with H2SO4 and HNO3 to produce α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula Q). More specifically, α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula Q) is prepared from α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) by first charging an Erlen-Meyer flask with H2SO4. The flask is then cooled in an ice bath and 50% HNO3 is added to the flask. The solid α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) is then added to the mixture in portions which maintain the temperature under 28° C. The reaction is then heated to 60° C. with stirring until a clear solution is obtained. When the reaction is complete, it is cooled to and maintained at room temperature. Water is then added to quench the reaction. The resulting slurry is cooled in an ice bath and then filtered to obtain α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula Q). See also Example 18 herein.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705033B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-f0db30901b7740e29a690caf37d305fa
Quellennotizuspto-grants-2010_04