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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic acid--water (1/1)HCID 21899381—
Edukt(S)-di-tert-butyl-5-cyanopyrrolidine-1,2-dicarboxylateHCID 131734566—
KatalysatorHydroxy-nickelHCID 444642—
LösungsmittelWaterHCID 962—
Produkt(S)-di-tert-butyl-5-formylpyrrolidine-1,2-dicarboxylateHCID 13173456551%

Reaktionsbedingungen

Temperatur80 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242985B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-4dbdd949243b43deaf76b6a27f3f2494
Quellennotizuspto-grants-2016_01