HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64385Erstellt: 24. Oktober 2026
1-Butanol → 5alpha-Hydroxy-6beta-(3-aminopropylamino)-cholestan-3beta-ol
https://huagongshe.com/de/reaction/64385
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | 1,3-Propanediamine | HCID 428 | — |
| Edukt | 6a-Cholesterol oxide | HCID 188855 | — |
| Lösungsmittel | tert-Butyl methyl ether | HCID 15413 | — |
| Produkt | 5alpha-Hydroxy-6beta-(3-aminopropylamino)-cholestan-3beta-ol | HCID 117642541 | 60% |
Reaktionsschritte
5,6α-epoxicholestan-3β-ol (8.9 g, 22.1 mmol, 1 eq) and 1,3-diaminopropane (3.3 g, 44.1 mmol, 2 eq) were charged in a round-bottomed flask equipped with a magnetic stirrer bar. 1-Butanol (70 ml, 5 vol) was added and the mixture heated to reflux for 40 h. The reaction mixture was cooled at r.t., diluted with methyl-tertbutyl-ether (5 vol) and washed with water (5 vol) and with brine (5 vol). The organic layer was passed through a silica pad (40 g) eluted with methyl-tertbutyl-ether (3 vol) then 10% Methanol/ethyl acetate (60 vol). Fractions of interest were pooled and the solvent was removed under reduced pressure to give 5α-Hydroxy-6β-(3-aminopropylamino)-cholestan-3β-ol as a white solid (6.3 g, 60%). In same conditions, use of ethanol as solvent (40 vol) and Ca(OTf)2 as catalyst gave a 20% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447141B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-13a252a6ba8e4d52861d8c41df587bfb |
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| Quellennotiz | uspto-grants-2016_09 |
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