HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58836Erstellt: 25. Oktober 2026
Imidazole → methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoate
https://huagongshe.com/reaction/58836
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Imidazole | HCID 795 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Iodide Ion | HCID 30165 | — |
| Edukt | N-Boc-L-serine methyl ester | HCID 7019177 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoate | HCID 10903591 | 68,1% |
Reaktionsschritte
A mixture of triphenylphosphine (131 g, 0.500 mol) and imidazole (34 g, 0.50 mol) in DCM (600 mL) was cooled to 0° C. and iodide (127 g, 0.50 mol) was added in small portions over 0.5 h. The cooling bath was removed and the mixture was stirred for 0.5 h. After the mixture was re-cooled to 0° C., a solution of (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate (73 g, 0.33 mol) in DCM (300 mL) was added dropwise. After the addition, the cooling bath was removed and the mixture was allowed to warm to ambient temperature and stirred for 1.5 h. The mixture was filtered and the filtrate was concentrated to remove most of the solvent. MTBE (400 mL) was added to the residue and the mixture was filtered to remove triphenylphosphine oxide. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel to afford (R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (74.0 g, 68% yield) as a colorless solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434761B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-c4c62557219c49f4894c4f195aa68a46 |
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| Quellennotiz | uspto-grants-2016_09 |
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