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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 360030Erstellt: 26. Oktober 2026

Water → tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoate

https://huagongshe.com/reaction/360030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiethyl EtherHCID 3283—
EduktTetrabutylammonium FluorideHCID 2724141—
EduktHexanoic acid, 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxo-, 1,1-dimethylethyl ester, (R)-(9CI)HCID 15045171—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of crude (R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3oxohexanoate, 43 g (0.126 mol) in 350 mL of tetrahydrofuran is treated with 213 mL of tetrabutylammonium fluoride solution (1.0 M in hexane). The resulting mixture is stirred for five hours, at 25° C. The mixture is treated with 500 mL of water, 300 mL of diethyl ether is added, and the layers separated. The organic layer is dried (magnesium sulfate) and then filtered through a plug of silica gel with the aid of anhydrous diethyl ether. The solvent is removed under a vacuum to obtain 21 g of crude (R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate with acceptable NMR, MS and IR spectra.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05003080
Quelldatensatzuspto-grants-1991_03
ORD IDord-58f5e643b0c34929a98f180ed8cea65e
Quellennotizuspto-grants-1991_03