HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 594832Erstellt: 25. Oktober 2026
Acetic acid--water (1/1) → (S)-di-tert-butyl-5-formylpyrrolidine-1,2-dicarboxylate
https://huagongshe.com/reaction/594832
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic acid--water (1/1) | HCID 21899381 | — |
| Edukt | (S)-di-tert-butyl-5-cyanopyrrolidine-1,2-dicarboxylate | HCID 131734566 | — |
| Katalysator | Hydroxy-nickel | HCID 444642 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (S)-di-tert-butyl-5-formylpyrrolidine-1,2-dicarboxylate | HCID 131734565 | 51% |
Reaktionsschritte
90 g Raney-Ni/H2O (50 w % in water, Acros) was added to a solution of 17.905 g (60.42 mmol) of the cyanide 110 in 640 ml Py/AcOH/H2O (2:1:1) and stirred under hydrogen for 72 h at 80° C. 300 ml water was added to the suspension, and the suspension was extracted 3× with 800 ml MTBE each. The combined organic phases were washed twice with water, dried over magnesium sulfate, and the solvent was removed at reduced pressure. The residue was filtered with 1000 ml EtOAc/CyHex (1:1) over silica gel, and, following the removal of the solvent, the raw product was purified by chromatography on silica gel with EtOAc/CyHex 1:4 as eluent. 9.234 g (30.85 mmol, 51%) of the aldehyde 111 was obtained as yellow oil (d.r.: 1.7:1 cis:trans).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242985B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-4dbdd949243b43deaf76b6a27f3f2494 |
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| Quellennotiz | uspto-grants-2016_01 |
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