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HRID 488111作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物1-AcetylpiperidineHCID 12058—
反応物Lithium diisopropylamideHCID 2724682—
反応物Ethyl (3R)-4-cyano-3-hydroxybutanoateHCID 2733879—
溶媒Tetrahydrofuran heptaneHCID 21263495—
生成物(R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrileHCID 22851143—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298627
出典データセットuspto-grants-1994_03
ORD IDord-47b878ee2d1f4cdf92f13e887b431019
出典メモuspto-grants-1994_03