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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383162생성일: 2026년 10월 25일

Hydrochloric Acid → (2S)-2-(((tert-butoxy)carbonyl)amino)-4-cyclohexylbutanoic acid

https://huagongshe.com/reaction/383162

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물1,4-DioxaneHCID 31275—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물(2S)-2-(((tert-butoxy)carbonyl)amino)-4-phenylbutanoic acidHCID 7018726—
촉매Platinum hydrochloric acidHCID 150198—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(2S)-2-(((tert-butoxy)carbonyl)amino)-4-cyclohexylbutanoic acidHCID 22862476106%

반응 조건

온도70 °C

반응 단계

To a solution of Boc-homophenylalanine (3.00 g, 10.8 mmol) in CH2Cl2 at room temperature was added a solution of 4N HCl in dioxane (20 mL, 80 mmol), and mixture stirred overnight. Solvents concentrated, and white powder that resulted was reduced under high pressure (4 atm. H2) using platinum/HCl. The white solid that resulted from the reduction was mixed with aqueous 4N NaOH (30 mL), water (30 mL), and THF (50 mL) at room temperature, and to this was added di-t-butyl dicarbonate (3.5 g, 16 mmol). Reaction heated at 70° C. overnight. Reaction cooled to 0° C., and an aqueous solution of 3N HCl added until the pH reached 6. Product extracted out with CHCl3, and extracts dried with Na2SO4, filtered, and concentrated in vacuo to produce a white solid (3.24 g, 106%). m/e (DCI) 286 (MH+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310095B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-9c42513025ff49dba74ab9f6c43a8dd9
출처 메모uspto-grants-2001_10