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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53988Erstellt: 25. Oktober 2026

4-Hydroxybenzaldehyde → 4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]benzaldehyde

https://huagongshe.com/reaction/53988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukttert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]benzaldehydeHCID 1177903999,7%

Reaktionsschritte

In 40 ml of tetrahydrofuran were dissolved 1.31 g of p-hydroxybenzaldehyde, 1.87 g of (3R)-1-tert-butoxycarbonyl-3-hydroxypyrrolidine and 2.88 g of triphenylphosphine. With stirring at room temperature, 1.91 g of diethyl azodicarboxylate was added to the thus prepared solution, and the mixture was stirred for 45 minutes. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a benzene/ethyl acetate mixture as an elution solvent. In this way, 2.9 g of 4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]benzaldehyde was obtained in an oily form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620991
Quelldatensatzuspto-grants-1997_04
ORD IDord-8b25371a6cf241ff8cbc0413b1a5ceab
Quellennotizuspto-grants-1997_04