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HRID 383162作成日:2026年10月26日

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

https://huagongshe.com/reaction/383162

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Sodium HydroxideHCID 14798—
反応物1,4-DioxaneHCID 31275—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物(2S)-2-(((tert-butoxy)carbonyl)amino)-4-phenylbutanoic acidHCID 7018726—
触媒Platinum hydrochloric acidHCID 150198—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物(2S)-2-(((tert-butoxy)carbonyl)amino)-4-cyclohexylbutanoic acidHCID 22862476106%

反応条件

温度70 °C

反応手順

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+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310095B1
出典データセットuspto-grants-2001_10
ORD IDord-9c42513025ff49dba74ab9f6c43a8dd9
出典メモuspto-grants-2001_10