Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfur trioxide-pyridine | HCID 168533 | — |
| Reactant | HCID 15391224 | HCID 15391224 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 54383698 | HCID 54383698 | 74% |
Reaction Steps
To a solution of N-benzyloxycarbonyl-(L)-phenylalanyl-(L)-tryptophanol (0.60 g) and triethylamine (0.53 ml) in dimethyl sulfoxide (DMSO) (7 ml), a solution of pyridine-sulfur trioxide complex (pyridine.SO3) in DMSO (7 ml) was added drop by drop. After stirring at room temperature for 1 hour, the reaction mixture was poured over ice water and extracted with ethyl ether (60 ml×3). The ethyl ether layer was washed by sequential additions of a 10% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution and saturated saline and then dried (MgSO4). After the solvent was distilled off, the residue was solidified from THF-hexane-ethyl ether to yield N-benzyloxycarbonyl-(L)-phenylalanyl-(L)-tryptophanal (0.44 g, 74%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05716980 |
|---|
| Source dataset | uspto-grants-1998_02 |
|---|
| ORD ID | ord-fb28b61abc4049ccbe48e0ce6f211752 |
|---|
| Source note | uspto-grants-1998_02 |
|---|