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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10129Erstellt: 23. Oktober 2026

Pyridine → (S)-6-benzoyloxy-3-oxo-5-hydroxyhexanoic acid tert-butylester

https://huagongshe.com/de/reaction/10129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzoyl chlorideHCID 7412—
EduktSodium HydroxideHCID 14798—
Edukt(5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl esterHCID 11401693—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-6-benzoyloxy-3-oxo-5-hydroxyhexanoic acid tert-butylesterHCID 1509984978%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 16.8 g (77 mmol) of the (5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl ester produced in Example 1 in 120 mL of methylene chloride were added 11.2 mL of pyridine and 10.2 mL of benzoyl chloride at 0° C., and the mixture was stirred at 0° C. for 2 hours. After completion of the reaction, the reaction mixture was diluted with 38 mL of water and adjusted to pH 7 with 20% aqueous NaOH solution. The aqueous layer was separated and further extracted with 2 portions of methylene chloride, 120 mL each. The organic layers were combined and dehydrated over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure to give an oil. This residue was purified by silica gel column chromatography (Kieselgel 60, product of Merck; hexane:acetone=5:1) to give 19.3 g of (5S)-6-benzoyloxy-5-hydroxy-3-oxohexanoic tert-butyl ester (white solid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094594B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-29050331286246aa9b5102f1f43d720f
Quellennotizuspto-grants-2006_08