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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477007Erstellt: 24. Oktober 2026

Hexane → 1-Phenyl-8-(2-tetrahydropyranyloxy)-1-octyne

https://huagongshe.com/de/reaction/477007

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktPhenylacetyleneHCID 10821—
Edukt2-[(6-bromohexyl)oxy]tetrahydro-2H-pyranHCID 103860—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexamethylphosphoramideHCID 12679—
Produkt1-Phenyl-8-(2-tetrahydropyranyloxy)-1-octyneHCID 1483422058,3%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a solution of 11.2 g of phenylacetylene dissolved in 100 ml of tetrahydrofuran, 78.8 ml of 1.6M-hexane solution of n-butyl lithium was added dropwise at 5°-8° C. Then 150 ml of a hexamethylphosphoramide solution containing 29.4 g of 1-bromo-6-(2-tetrahydropyranyloxy)-hexane was added dropwise at 10°-20° C. After stirring at 20° C. for 30 minutes, the reaction mixture was poured into ice-water and extracted with hexane. The organic layer was washed with water, dried and then the organic solvent was distilled off. The residue was purified by silica gel column chromatography (solvent: hexane-ethyl acetate=10:1), to give 18.3 g of 1-phenyl-8-(2-tetrahydropyranyloxy)-1-octyne as an oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04886817
Quelldatensatzuspto-grants-1989_12
ORD IDord-5198d37285e94e4c917601bdb7bb3bf0
Quellennotizuspto-grants-1989_12