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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253579Erstellt: 25. Oktober 2026

D-Proline → HCID 57786523, Verbindung

https://huagongshe.com/reaction/253579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktD-ProlineHCID 8988—
Edukt1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
EduktSodium borohydrideHCID 4311764—
Edukt3-(Oxan-4-yl)propanalHCID 57449683—
LösungsmittelEthanolHCID 702—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 57786523HCID 5778652389%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 3-(tetrahydro-pyran-4-yl)-propionaldehyde (8.59 g, 0.06 mol) and dibenzyl azodicarboxylate (12.8 g, 0.042 mol) in MeCN (250 mL) at 0° C. was added (R-proline) (0.48 g, 0.0042 mol). After stirring the mixture at 0° C. for 15 h, ethanol (100 mL) and NaBH4 (1.56 g, 0.042 mol) were added, and the mixture was stirred at 0° C. for 40 min. The reaction was quenched by slow addition of 10% aq citric acid (15 mL), and the whole solution was concentrated in vacuo. This residue was diluted with EtOAc (200 mL), washed with brine (50 mL), dried over Na2SO4, and concentrated in vacuo to give crude product which was purified by column chromatography to give (S)-dibenzyl 1-(1-hydroxy-3-(tetrahydro-2H-pyran-4-yl)propan-2-yl)hydrazine-1,2-dicarboxylate (16.52 g, 89%). 1H NMR (CD3OD) δ 1.0-1.5 (m, 8H), 2.9-3.3 (m, 2H), 3.4-3.6 (m, 2H), 3.7-3.9 (m, 2H), 4.4-4.7 (m, 2H), 5.1-5.4 (m, 4H), 7.2-7.4 (m, 10H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872028B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-e081292ec63447d6af8e1dcf1288bce3
Quellennotizuspto-grants-2011_01