Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Boc-3,4-difluoro-D-phenylalanine | HCID 2736194 | — |
| Product | HCID 11041808 | HCID 11041808 | 58% |
Reaction Steps
Boc-D-3,4-Difluorophenylalanine (3.05 g, 11.0 mmol, 1 equiv) was dissolved in 1,4-dioxane (10 mL), and a solution of HCl in 1,4-dioxane (4.0 M, 10 mL) was added. The reaction was stirred at 23° C. for 5 h, then the solvent was removed under reduced pressure. The residue was dissolved in 1 M H2SO4 (22 mL), cooled to 0° C. and 2 N NaNO2 (22 mL) was added via addition funnel under argon. The reaction mixture was stirred at 0° C. for 3 h and warmed to room temperature overnight. The resulting mixture was extracted with MTBE (3×40 mL), dried over Na2SO4 and concentrated. The residue was recrystallized from ether/petroleum ether to afford the title intermediate (1.29 g, 58%) as off-white solid. 1H NMR (DMSO-d6) δ 0.82-0.86 (m, 2H), 1.10-1.27 (m, 4H), 1.40-1.48 (m, 2H), 1.63-1.78 (m, 5H), 3.95-4.00 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06514997B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-72f72ecb3ee647709c393daee85e8970 |
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| Source note | uspto-grants-2003_02 |
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