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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488111생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/488111

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물1-AcetylpiperidineHCID 12058—
반응물Lithium diisopropylamideHCID 2724682—
반응물Ethyl (3R)-4-cyano-3-hydroxybutanoateHCID 2733879—
용매Tetrahydrofuran heptaneHCID 21263495—
생성물(R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrileHCID 22851143—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298627
출처 데이터셋uspto-grants-1994_03
ORD IDord-47b878ee2d1f4cdf92f13e887b431019
출처 메모uspto-grants-1994_03