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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5711Generated: October 25, 2026

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

https://huagongshe.com/reaction/5711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHexanoic acid, 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxo-, 1,1-dimethylethyl ester, (R)-(9CI)HCID 15045171—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of crude (R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxohexanoate, 43 g (0.126 mol) in 350 mL of tetrahydrofuran is treated with 213 mL of tetrabutylammonium fluoride solution (1.0M 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245047
Source datasetuspto-grants-1993_09
ORD IDord-a9e5e1fe7109474dbd63453d82efc8ef
Source noteuspto-grants-1993_09