HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59775Erstellt: 23. Oktober 2026
3-Furancarboxaldehyde, tetrahydro- → HCID 178424141, Verbindung
https://huagongshe.com/de/reaction/59775
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | HCID 178424139 | HCID 178424139 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | HCID 178424141 | HCID 178424141 | — |
| Produkt | HCID 178424142 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09440941B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-49890fe6d6d0441ab752901cbf80fecd |
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| Quellennotiz | uspto-grants-2016_09 |
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