Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 20821099 | HCID 20821099 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Acetyl-L-phenylalanine | HCID 6420123 | — |
Reaction Steps
Fmoc-4-acetyl-L-phenylalanine was purchased from RSP Amino Acid Analogues, Inc. (Worcester, Mass.). This compound (1.0 g, 2.3 mmol) was stirred with 4 mL of piperidine (20% in DMP) for 2 hours at room temperature. The solvent was evaporated to obtain white powder. The solid was then resuspended in 10 mL of cold water (0.1% TFA), and the supernatant was collected by filtration. Preparative reverse-phase HPLC (Microsorb C18, Rainin Instrument Co., Inc., Woburn, Mass.) was used to separate the desired product from the reaction mixture (5-30% CH3CN in H2O with 0.1% TFA over 30 min). The eluant (tR=12 min) was lyophilized to a obtain white solid (0.45 g, 88%). 1HNMR (D2O): δ 7.85-7.28 (m, 4H), 4.23 (dd, 1H, 5.4 Hz), 3.2 (m, 2H), 2.7 (s, 3H). LRMS, calcd for C11H13NO3 (M++1): 208.09. Found (ESI): 208.47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07910345B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-8c2ac949a58d4e4ba2506792351946dc |
|---|
| Source note | uspto-grants-2011_03 |
|---|