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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktTriphenylphosphineHCID 11776—
EduktIodide IonHCID 30165—
EduktN-Boc-L-serine methyl esterHCID 7019177—
LösungsmittelDichloromethaneHCID 6344—
Produktmethyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 1090359168,1%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434761B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-c4c62557219c49f4894c4f195aa68a46
Quellennotizuspto-grants-2016_09