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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | proline dl-form | HCID 614 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Trimethylsilyldiazomethane | HCID 167693 | — |
| Edukt | (2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid | HCID 58714586 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07189754B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-d1b970716bbc4b3c94fe462585b988e2 |
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| Quellennotiz | uspto-grants-2007_03 |
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