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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488110생성일: 2026년 10월 26일

Hydrochloric Acid → (R)-6-cyano-N-(1,1-dimethylethyl)-5-hydroxy-3-oxo-N-(phenylmethyl)hexanamide

https://huagongshe.com/reaction/488110

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물N-BenzylacetamideHCID 11500—
반응물Lithium diisopropylamideHCID 2724682—
반응물Ethyl (3R)-4-cyano-3-hydroxybutanoateHCID 2733879—
용매Tetrahydrofuran heptaneHCID 21263495—
생성물(R)-6-cyano-N-(1,1-dimethylethyl)-5-hydroxy-3-oxo-N-(phenylmethyl)hexanamideHCID 53869197—

반응 단계

To a stirred -10° C. solution of N-1,1-dimethyl-ethyl, N-phenylmethylacetamide (prepared from N-1,1-dimethylethyl, N-phenylmethyl amine, and acetyl chloride by refluxing for 2 hours in toluene) (102.5 g, 0.5 mol) in tetrahydrofuran (0.5 L) is slowly added a solution of lithium diisopropylamide in tetrahydrofuran-heptane (0.25 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) (20 g, 0.125 mol) as a solution in 200 mL or 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 (0.5 L). The aqueous layer is extracted with 300 mL of ethyl acetate, the aqueous layer is separated and reextracted with 100 mL of ethyl acetate, the extracts are combined and concentrated in vacuo to afford crude (R)-6-cyano-N-(1,1-dimethylethyl)-5-hydroxy-3-oxo-N-(phenylmethyl)hexanamide as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298627
출처 데이터셋uspto-grants-1994_03
ORD IDord-ab378d00d9d4494796b6c0db5e6972e8
출처 메모uspto-grants-1994_03