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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436979Erstellt: 25. Oktober 2026

Acetic Anhydride → 3-Cyclohexen-1-ol, 3,5,5-trimethyl-, acetate

https://huagongshe.com/reaction/436979

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktBeta-IsophoroneHCID 10108—
EduktSodium AcetateHCID 517045—
EduktSodium borohydrideHCID 4311764—
Edukt3,5,5-Trimethylcyclohex-3-en-1-olHCID 11275049—
LösungsmittelMethanolHCID 887—
Produkt3-Cyclohexen-1-ol, 3,5,5-trimethyl-, acetateHCID 90791—

Reaktionsschritte

Prepared by reduction by means of sodium borohydride in methanol of β-isophorone [obtained according to J. Am. Chem. Soc., 63, 2308 (1941)] and subsequent acetylation of the obtained 3,5,5-trimethyl-cyclohex-3-en-1-ol by means of acetic anhydride in the presence of sodium acetate at 50° C. during 20 hours.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04029108
Quelldatensatzuspto-grants-1977_06
ORD IDord-f7e2abb6699d49ea804fb4d000f108d2
Quellennotizuspto-grants-1977_06