HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → O-benzyl-N-trifluoroacetyltyrosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl trifluoroacetate | HCID 9893 | — |
| Reactant | O-benzyl-L-tyrosine | HCID 725701 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | O-benzyl-N-trifluoroacetyltyrosine | HCID 53698430 | — |
Reaction Steps
112.5 g (0.41 mmol) of O-benzyltyrosine is suspended in 1 liter of dry methanol and mixed at room temperature with 58.9 ml (0.42 mol) of triethylamine. After addition of 67 ml (0.53 mol) of trifluoroacetic acid methyl ester, it is stirred for 130 hours at room temperature with exclusion of water. The unreacted initial material is separated and the leaving components are removed by shaking with ethyl acetate/aqueous hydrochloric acid. The ethyl acetate phase is decolored with activated carbon. After evaporation of the solvent, 120.7 g (80% of theory) of colorless crystals is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05681543 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-8ce287e9123b42a0bbba7acbe5493f05 |
| Source note | uspto-grants-1997_10 |