HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetic acid, 2-fluoro-, 1,1'-anhydride | HCID 67886 | — |
| Reactant | N-(tert-butoxycarbonyl)-L-aspartic acid | HCID 99718 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid | HCID 10131156 | — |
Reaction Steps
A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05416013 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-1f37921e0a2e4e799336bdb217625c12 |
| Source note | uspto-grants-1995_05 |