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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 457919Erstellt: 24. Oktober 2026

proline dl-form → 1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate

https://huagongshe.com/de/reaction/457919

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktproline dl-formHCID 614—
EduktMethanolHCID 887—
EduktTrimethylsilyldiazomethaneHCID 167693—
Edukt(2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acidHCID 58714586—
LösungsmittelTolueneHCID 1140—
Produkt1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylateHCID 58585478—

Reaktionsschritte

A solution of the oximether- and/or olefin-type 2-pyrrolidinecarboxylic acid intermediate, e.g. (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid (0.648 g, 2.5 mmol), in a 1:1 mixture of methanol and toluene (35 ml) was made. Trimethylsilyl diazomethane (3.8 ml of a 2M solution in hexanes, 7.5 mmol) was then added dropwise to the stirred solution at room temperature under nitrogen. After completion of the evolution of nitrogen gas, the resulting yellow solution was evaporated in vacuo, and the residue filtered through a pad of silica gel, eluting with ethyl acetate. Removal of solvent from the filtrate gave the methylester product, e.g. 1-tert-butyl 2-methyl(2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate, as a yellow oil (0.646 g, 95% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189754B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-d1b970716bbc4b3c94fe462585b988e2
Quellennotizuspto-grants-2007_03