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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383162Generated: October 25, 2026

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

https://huagongshe.com/reaction/383162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-4-phenylbutanoic acidHCID 7018726—
CatalystPlatinum hydrochloric acidHCID 150198—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(2S)-2-(((tert-butoxy)carbonyl)amino)-4-cyclohexylbutanoic acidHCID 22862476106%

Reaction Conditions

Temperature70 °C

Reaction Steps

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+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310095B1
Source datasetuspto-grants-2001_10
ORD IDord-9c42513025ff49dba74ab9f6c43a8dd9
Source noteuspto-grants-2001_10