HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → O-benzyl-N-trifluoroacetyltyrosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| 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 combined at room temperature with 58.9 ml (0.42 mol) of triethylamine. After adding 67 ml (0.53 mol) of trifluoroacetic acid ethyl ester, the mixture is stirred at room temperature for 130 hours under exclusion of moisture. The mixture is separated from unreacted starting material and volatile components are removed by shaking with ethyl acetate/aqueous hydrochloric acid. The ethyl acetate phase is decolorized with activated carbon. Evaporation of the solvents yields 120.7 g (80% of theory) of colorless crystals. Melting point: 149°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05482700 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-fbd95790bc8a46c48bfb733137faeec6 |
| Source note | uspto-grants-1996_01 |