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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62904Erstellt: 26. Oktober 2026

Hydrogen Peroxide → 2-(4-Benzyloxy-3,5-difluoro-phenyl)-cyclopropanecarboxylic acid

https://huagongshe.com/reaction/62904

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktLithium HydroxideHCID 3939—
EduktSodium SulfiteHCID 24437—
EduktOxolane--water (1/1)HCID 21881883—
Edukt(R)-4-benzyl-3-[2-(4-benzyloxy-3,5-difluoro-phenyl)-cyclopropanecarbonyl]-oxazolidin-2-onHCID 90118118—
LösungsmittelWaterHCID 962—
Produkt2-(4-Benzyloxy-3,5-difluoro-phenyl)-cyclopropanecarboxylic acidHCID 90118240—

Reaktionsschritte

After LiOH (6.4 mg, 0.152 mmol) was dissolved in water (1 mL), H2O2 (35%, 37 mg, 0.38 mmol) was added thereto, and the mixture was stirred at room temperature for 30 minutes, and then cooled to 0° C. The reactant was added to the solution of (R)-4-benzyl-3-[2-(4-benzyloxy-3,5-difluoro-phenyl)-cyclopropanecarbonyl]-oxazolidin-2-on (less polar, 44 mg, 0.095 mmol) obtained in Step B of Preparation Example 58 dissolved in THF/H2O (2 mL/0.5 mL), and the mixture was stirred for 1 hour. After the termination of the reaction, Na2SO3 solution (0.1 g in 1 mL of H2O) was added thereto, and the mixture was stirred at 0° C. for 1 hour, and then concentrated under reduced pressure. The residue was added with water, and 6N HCl aqueous solution was added to adjust the pH of the solution to 2. The organic layer obtained by the extraction with ethyl acetate was separated, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain the mixture (41 mg) of the title compound and 4-benzyloxazolidin-2-on, which was used in the next step without a separate purification process.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447044B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-57d96369d3eb427788d6186785596aa0
Quellennotizuspto-grants-2016_09