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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25788Erstellt: 25. Oktober 2026

Cyclohexane, (bromomethyl)- → 4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/25788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexane, (bromomethyl)-HCID 137636—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt4-(1-Cyclohexylmethoxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 69190771—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinolineHCID 1031667025,6%

Reaktionsschritte

4-(1-Cyclohexylmethoxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester (70 mg) was treated with 255 μL of 1 M solution of sodium bis(trimethylsilyl)amide in THF and 45 mg of cyclohexylmethyl bromide to give the alkylated product, which was deprotected to yield 8 mg of the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858627B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-44529c863784495ba0268ab73cd417bc
Quellennotizuspto-grants-2005_02