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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721458Generated: October 26, 2026

Hydrochloric Acid → (R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrile

https://huagongshe.com/reaction/1721458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant1-AcetylpiperidineHCID 12058—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl (3R)-4-cyano-3-hydroxybutanoateHCID 2733879—
SolventTetrahydrofuran heptaneHCID 21263495—
Product(R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrileHCID 22851143—

Reaction Steps

To a stirred -10° C. solution of 1-acetylpiperidine (127 g, 1.0 mol) in tetrahydrofuran (1.0 L) is slowly added a solution of lithium diisopropylamide in tetrahydrofuran-heptane (0.5 L of 2M) while maintaining the temperature between -40° C. to -50° C., and the mixture is stirred at -20° C. to -30° C. for 30 minutes. (R)-4-cyano-3-hydroxybutyric acid, ethyl ester (Brower, supra) (40 g, 0.25 mol) as a solution in 200 mL of tetrahydrofuran is then added to the previous mixture. The reaction mixture is stirred for 30 minutes at -25° C. to -20° C., and transferred to a 2.2N aqueous hydrochloric acid solution (1 L) . The aqueous layer is extracted with 500 mL of ethyl acetate, the aqueous layer is separated and extracted with 100 mL of ethyl acetate, the extracts are combined and concentrated in vacuo to afford (R)-ε-hydroxy-α,γ-dioxo-1-piperidineheptanenitrile as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510488
Source datasetuspto-grants-1996_04
ORD IDord-e9a3a0c7c7454c958c738cc5f57d2558
Source noteuspto-grants-1996_04