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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 334834Erstellt: 23. Oktober 2026

2-Ethylhexanoic Acid → 2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl ester

https://huagongshe.com/de/reaction/334834

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Ethylhexanoic AcidHCID 8697—
EduktSodium CarbonateHCID 10340—
Edukt2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenolHCID 54751948—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl esterHCID 6729622389%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol (10.0 g, 33 mmol) is suspended in a mixture of 2-ethylhexanoic acid (11.9 g, 82 mmol) and tetrahydrofuran (75 g) and stirred at 70° C. for 30 minutes. Sodium carbonate (10.5 g, 99 mmol) is added. The slightly yellow reaction mixture is stirred at 60° C. for 15 minutes and evaporated to dryness. The residue is dissolved in ethyl acetate and extracted with an aqueous potassium carbonate solution (10%) and brine. The organic layer is dried over sodium sulphate, filtered and evaporated to dryness. The crude product is purified by column chromatography (ethyl acetate/heptane 1:12) to yield 11.2 g of 2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883829B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-6cd398ffc4d44d75bea72023ea05bf74
Quellennotizuspto-grants-2014_11