HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → N-Boc-5-Iodo-L-norvaline tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate | HCID 10062769 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Boc-5-Iodo-L-norvaline tert-butyl ester | HCID 15479354 | — |
Reaction Steps
To a solution of t-butyl (S)-5-hydroxy-2-(t-butoxycarbonylamino)-pentanoate (5.79 g, 20.0 mmol), triphenylphosphine (8.13 g, 31.0 mmol) and imidazole (2.04 g, 30.0 mmol) in CH2Cl2 (200 mL) at room temperature is added iodine (6.35 g, 25.0 mmol), portionwise, over 30 minutes. The mixture is then stirred 16 hours at room temperature. Methanol (20 mL) is added to the solution, which is then stirred an additional 1 hour. Solvent is evaporated, and the residue is purified by chromatography (silica, 33% EtOAc/hexane) to yield t-butyl (S)-5-iodo-2-(t-butoxycarbonylamino)-pentanoate as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353017B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-7c6289faa39441d3824ed62cc75a584e |
| Source note | uspto-grants-2002_03 |