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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893506Generated: October 26, 2026

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

https://huagongshe.com/reaction/893506

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 tetrahydro-furan 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-dimethyl-ethyl 6-cyano-5-hydroxy-3-oxohexanoate with acceptable NMR, MS and IR spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05124482
Source datasetuspto-grants-1992_06
ORD IDord-b85808d5726947fe8aff9e1f181bc73a
Source noteuspto-grants-1992_06