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HRID 237820Erstellt: 26. Oktober 2026

(4-Methoxy-2-methylphenyl)boronic acid → 3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflate

https://huagongshe.com/reaction/237820

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Methoxy-2-methylphenyl)boronic acidHCID 2773486—
Edukt3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflateHCID 11087380—
Produkt3,3,5,5-Tetramethylcyclohex-1-en-1-yl triflateHCID 11087380—
Produkt4-Methoxy-2-methyl-1-(3,3,5,5-tetramethyl-cyclohex-1-enyl)-benzeneHCID 68525758—

Reaktionsschritte

Trifluoro-methanesulfonic acid 3,3,5,5-tetramethyl-cyclohex-1-enyl ester was prepared in accordance with the procedures of Hanack et. al., J. Heterocyclic Chem. 1988, 25, pp 1237-1241. 4-Methoxy-2-methyl-1-(3,3,5,5-tetramethyl-cyclohex-1-enyl)-benzene was prepared in two steps by a Suzuki coupling of 4-methoxy-2-methyl-phenylboronic acid and trifluoro-methanesulfonic acid 3,3,5,5-tetramethyl-cyclohex-1-enyl ester following the procedures of Carmen et. al., Synlett 2005, No. 10, pp 1601-1605, to obtain 4-methoxy-2-methyl-1-(3,3,5,5-tetramethyl-cyclohex-1-enyl)-benzene, which was subsequently hydrogenated to form 1-cyclohexyl-4-methoxy-2-methyl-benzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642603B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-d6abbe0e348b420ea39320bc603c75fb
Quellennotizuspto-grants-2014_02