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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655078Erstellt: 25. Oktober 2026

Lilial → (E)-3(2-Hydroxy-phenyl)-acrylic acid 3(4-tert-butyl-phenyl)-1-ethoxy-propyl ester

https://huagongshe.com/reaction/655078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLilialHCID 228987—
Edukt(E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acidHCID 22290462—
Edukt1-Tert-butyl-4-(3-ethoxy-2-methyl-allyl)-benzeneHCID 54077483—
Katalysatorp-Toluenesulfonic acidHCID 6101—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(E)-3(2-Hydroxy-phenyl)-acrylic acid 3(4-tert-butyl-phenyl)-1-ethoxy-propyl esterHCID 6852321528,2%

Reaktionsschritte

A solution of 3.1 g of (E)-3-[2-(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid, 3.0 g of 1-tert-butyl-4-(3-ethoxy-2-methyl-allyl)-benzene, accessible from 3-(4-tert-butyl-phenyl)-2-methyl-propionaldehyde via a two step procedure according to P. D. Bartlett and A A. Frimer, Heterocycles 11, 419-435, (1978), and 20 mg of p-TSA in 25 ml of toluene was stirred at 0° C. for 4 h and at room temperature for 14 h. The reaction mixture was partitioned between saturated sodium carbonate and hexane and the organic layer was washed with brine, dried over (Na2SO4) and evaporated to dryness to yield 5.3 g of the crude intermediate (E)-3-[2-(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid 3-(4-tert-butyl-phenyl)-1-ethoxy-propyl ester as a pale yellow oil. This was dissolved in 20 ml of THF and treated at 0° C. with 3.2 g of solid TBAF-3H2O. After 30 min., the mixture was concentrated and purification by repeated flash chromatography yielded 1.2 g of the title ester (a mixture of diastereoisomers) as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE043006E1
Quelldatensatzuspto-grants-2011_12
ORD IDord-5fc8dd8969f5410f93583b2e57cc2393
Quellennotizuspto-grants-2011_12