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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | (2S)-2-(((tert-butoxy)carbonyl)amino)-4-phenylbutanoic acid | HCID 7018726 | — |
| Catalyst | Platinum hydrochloric acid | HCID 150198 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-2-(((tert-butoxy)carbonyl)amino)-4-cyclohexylbutanoic acid | HCID 22862476 | 106% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310095B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-9c42513025ff49dba74ab9f6c43a8dd9 |
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| Source note | uspto-grants-2001_10 |
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