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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59775Erstellt: 23. Oktober 2026

3-Furancarboxaldehyde, tetrahydro- → HCID 178424141, Verbindung

https://huagongshe.com/de/reaction/59775

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Furancarboxaldehyde, tetrahydro-HCID 157568—
EduktSodium cyanoborohydrideHCID 5003444—
EduktHCID 178424139HCID 178424139—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelSodium BicarbonateHCID 516892—
ProduktHCID 178424141HCID 178424141—
ProduktHCID 178424142HCID 178424142—

Reaktionsschritte

To a solution of 61 mg trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexylamine (0.18 mmol) in 3 ml methanol and 0.2 ml of acetic acid at room temperature 39 mg tetrahydrofuran-3-carboxaldehyde (0.20 mmol) in 3 ml of methanol were added, and 12 mg of sodium cyanoborohydride (0.89 mmol (0.20 mmol) were then added in one portion. Stirring at room temperature was continued for 16 h. The solution was diluted with aqueous saturated sodium hydrogencarbonate solution and the aqueous layer extracted with dichloromethane. The combined organic layers were dried with sodium sulfate and filtered, and the solvent removed under reduced pressure. The crude product was purified by RP-HPLC. 23 mg of (tetrahydrofuran-3-ylmethyl)-[trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexyl]-amine and 19 mg of bis-(tetrahydrofuran-3-ylmethyl)-[trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexyl]-amine were isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440941B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-49890fe6d6d0441ab752901cbf80fecd
Quellennotizuspto-grants-2016_09