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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1452381Erstellt: 26. Oktober 2026

Ammonium Chloride → 5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran

https://huagongshe.com/reaction/1452381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktHeptyltriphenylphosphonium bromideHCID 2724567—
Edukt5-Acetoxy-4,6-di-tert-butyl-2-formylbenzofuranHCID 22918669—
EduktButyllithiumHCID 178418339—
LösungsmittelPentaneHCID 8003—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuranHCID 5376872197%

Reaktionsschritte

A pentane solution (6.0 ml) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium bromide (4.2 g) in tetrahydrofuran (30 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 90 min, a solution of 5-acetoxy-4,6-di-tert-butyl-2-formylbenzofuran (2.54 g) in tetrahydrofuran (20 ml) was added dropwise. Subsequently, the mixture was heated under reflux for 1 h and, after cooling, a saturated aqueous solution of ammonium chloride was added and the mixture was subjected to extraction with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2-(1-octenyl)benzofuran [3.1 g (yield, 97%)] as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05606089
Quelldatensatzuspto-grants-1997_02
ORD IDord-2ab65c6669334c7c813729a38036c741
Quellennotizuspto-grants-1997_02