Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1919771Erstellt: 26. Oktober 2026

Lithium Hydroxide → 5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pentan-2-ol

https://huagongshe.com/reaction/1919771

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium HydroxideHCID 3939—
Edukt5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetateHCID 59235133—
LösungsmittelMethanolHCID 887—
Produkt5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pentan-2-olHCID 5923503493,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A 2 mol/L Lithium hydroxide solution (2 mL) was added to a mixed solution of 5-[4-[1,1,1,3,3,3-hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetate (80.4 mg, 169 μmol) in methanol (1.5 mL) at room temperature, followed by heating at an external temperature of 60° C. in an oil bath overnight. After completion of the reaction, methanol was evaporated under reduced pressure. The pH was adjusted to 7 by adding 4 mol/L hydrochloric acid (2 mL) to the residue. After extraction with chloroform-water, the organic layer was washed with a saturated sodium chloride solution and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. 68.1 mg of the title compound (yield: 93%) was obtained as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08168666B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-243e2e93a5bf448ea8f5dd45ebf866c0
Quellennotizuspto-grants-2012_05