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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1761748Erstellt: 25. Oktober 2026

Hexanoic Acid → (-)-4-Octyloxy-4'-(1-hexanoyloxyethyl)biphenyl

https://huagongshe.com/reaction/1761748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexanoic AcidHCID 8892—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt(+)-4-Octyloxy-4'-(1-butanoyloxyethyl)biphenylHCID 19857772—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(-)-4-Octyloxy-4'-(1-hexanoyloxyethyl)biphenylHCID 1432389276,3%

Reaktionsschritte

Seven grammes (21 mmol) of (-)-1-(4-octyloxybiphenyl-4'-yl)ethanol prepared in Example 2, 7.5 g (36 mmol) of N,N'-dicyclohexylcarbodiimide and 1.0 g of 4-dimethylaminopyridine were dissolved in 200 ml of dichloromethane. To the solution, 3.4 g (29 mmol) of caproic acid was added and the mixture was stirred for six hours at room temperatre. The deposit crystals were filtered, 200 ml of water was added to the filtrate, and the organic layer was separated. 6N hydrochloric acid was added to the organic solution, and then the solution was neutralized with the aqueous solution of 2N sodium hydroxide. The neutralized solution was washed with water until the washed water became neutral. The solvent and low-boiling fractions were distilled off from the obtained solution. The residue was recrystallized from ethanol and the desired (-)-4-octyloxy-4'-(1-hexanoyloxyethyl)biphenyl 6.8 g was obtained. m.p. 60.8° C., [α]D -78.4° (c 0.88, C2H5OH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04827052
Quelldatensatzuspto-grants-1989_05
ORD IDord-6b0d047b83d8438c8acec340794c0b33
Quellennotizuspto-grants-1989_05