HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 574128Erstellt: 25. Oktober 2026
Tetrahydrofuran → 3-Hydroxymethyl-beta-carboline
https://huagongshe.com/reaction/574128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Methyl 9H-pyrido(3,4-b)indole-3-carboxylate | HCID 107704 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-Hydroxymethyl-beta-carboline | HCID 5353338 | — |
Reaktionsschritte
3-carbomethoxy-β-carboline or a derivative thereof (J in Scheme VII above) is dissolved in a polar solvent (e.g., THF), and a reducing agent (e.g., NaBH4) is added to the solution. The mixture is stirred for a few hours and cooled. An excess of water is then added, and the mixture is stirred for another few hours. The solvent is thereafter evaporated and the resulting residue is dissolved in water, washed several times with one or more non-polar solvents such as dichloromethane and ethyl acetate, and the combined organic extracts are then evaporated. The remaining residue is purified by column chromatography (e.g., on a silica gel with elution by a 9:1 mixture of ethylacetate and methanol), to give a 3-hydroxymethyl-β-carboline intermediate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09034872B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-ec33a9ffa6874c778560b7e2fa43f17d |
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| Quellennotiz | uspto-grants-2015_05 |
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