HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-((Methoxycarbonyl)methyl)4-Nitrophenylalanine Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Methyl 4-nitro-L-phenylalaninate hydrochloride | HCID 11715866 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-((Methoxycarbonyl)methyl)4-Nitrophenylalanine Methyl Ester | HCID 68574020 | 92% |
Reaction Steps
Triethylamine (22 mmol) was added to a suspension of 4-Nitrophenylalanine methyl ester hydrochloride (2) (21 mmol) in THF (50 ml). The mixture was stirred at room temperature for one hour, the triethylamine hydrochloride was filtered off, and the filtrate concentrated to yellow oil. The oil was dissolved in dry THF (50 ml) and to this solution was added triethylamine (60 mmol) and methylbromoacetate (60 mmol), the solution was stirred at room temperature under nitrogen atmosphere for 3 hours, after which the precipitate was filtered off and the filtrate concentrated on vacuum. The residue was dissolved in ethylacetate, washed with H2O, dried (MgSO4) and concentrated on vacuum to give yellow oil. The yield was 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132513B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-1d361a77553743f0b595134964d1542c |
| Source note | uspto-grants-2006_11 |