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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 409677Erstellt: 24. Oktober 2026

Acetaldehyde → HCID 69179394, Verbindung

https://huagongshe.com/de/reaction/409677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt4-(4-Nitrophenyl)piperidineHCID 15925817—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 69179394HCID 69179394—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

Sodium triacetoxyborohydride (3.1 g, 14.6 mmol, 3 equiv) is added to a cold (5° C.) solution of 4-(4-nitro-phenyl)-piperidine (1 g, 4.9 mmol) and acetaldehyde (0.82 mL, 14.6 mmol, 3 equiv) in DCM (20 mL). The reaction mixture is stirred for 1 h at 5° C. and then diluted with DCM and a saturated aqueous solution of NaHCO3. The layers are separated and the aqueous layer is extracted with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM/MeOH+1% NH3aq, 98:2) to provide the title compound as a yellow oil. ESI-MS: 235.1 [MH]+; tR=2.64 min (purity: 85%, system 1); TLC: Rf=0.14 (DCM/MeOH+1% NH3aq, 98:2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759517B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-994abab701f7404d89fd24d4e092ec07
Quellennotizuspto-grants-2014_06