HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 4-Nitrobenzoate | HCID 4419940 | — |
| Reactant | tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate | HCID 87514848 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoate | HCID 86683881 | 59.3% |
Reaction Steps
4-nitrobenzoate (16.3 g), triphenylphosphine (32 g), and diisopropyl azodicarboxylate (40% toluene solution) (64 ml) were added dropwise to a tetrahydrofuran (50 ml) solution containing tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate (17 g) for 30 minutes, followed by stirring at room temperature for 14 hours. The solvent was distilled away from the reaction solution under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5.5:1), and a yellow solid of (2S)-2-((tert-butoxycarbonyl)amino)hexane-3-yl 4-nitrobenzoate (17 g) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895585B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-44aa852be7c1423898b3a2ff746c57a8 |
| Source note | uspto-grants-2014_11 |