Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 17819417 | HCID 17819417 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 17819432 | HCID 17819432 | 89.5% |
Reaction Steps
A Parr bottle was charged with palladium (II) hydroxide (800 mg), a solution of N-butoxycarbonyl-1-iodo-2-amino-3-fluoro-3-methyl-n-butane (3.26 g, 9.8 mmol) in ethanol (80 mL) and triethylamine (0.99 g, 9.8 mmol). The reaction mixture was placed under hydrogen gas (50 psig) and shaken for 20 hours. The mixture was filtered through celite and evaporated. The residue was dissolved in diethyl ether (100 mL) and washed with 1N aq. HCl (2×50 mL), water (2×50 mL), and then dried (MgSO4). Filtration and evaporation gave a residue that was chromatographed (silica gel, diethyl ether/hexane (3/1)) to afford 1.80 g of N-butoxycarbonyl-2-amino-3-fluoro-3-methyl-n-butane: 1H NMR (CDCl3) δ 4.65 (br, 1H), 3.70 (br m, 1H), 1.45 (s, 9H), 1.39 (d, 3H), 1.32 (d, 3H) and 1.18 (d, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763474 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-539d3a22969342f18176a0345d2e512c |
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| Source note | uspto-grants-1998_06 |
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