HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Fmoc-l-tryptophanyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | Fmoc-L-tryptophan | HCID 978343 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Fmoc-l-tryptophanyl fluoride | HCID 11362381 | — |
Reaction Steps
FMOC-L-Tryptophan (5 g, 11.72 mmol) (Bachem) was dissolved in dichloromethane (60 mL). Pyridine (0.95 mL, 11.72 mmol) (Aldrich) and cyanuric fluoride (1.58 g, 11.72 mmol) (Aldrich) were successively added at room temperature and the mixture was stirred for 6.5 hours. Ice cold water (100 mL) was added and the resulting slurry was filtered. The filtrate was poured into a separatory funnel and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford FMOC-L-tryptophanyl fluoride as a beige powder. (Yield 4.36 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084270B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-0c4289f38f9b4359b0462549c3b30f31 |
| Source note | uspto-grants-2006_08 |