HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 580749Erstellt: 24. Oktober 2026
Triphenylphosphine → Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]-
https://huagongshe.com/de/reaction/580749
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 2-(2-(2-(2-Azidoethoxy)ethoxy)ethoxy)ethanol | HCID 4614742 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]- | HCID 160103 | — |
Reaktionsschritte
To a solution of Compound XXV (15.94 g; 72.7 mmole) in 100 ml of pyridine was added triphenylphosphine (29 g; 111 mmole). After stirring for one hour, at which time gas evolution had subsided, 50 ml of concentrated aqueous ammonium hydroxide was added and the mixture stirred overnight. The reaction mixture was concentrated under vacuum and the residue partitioned between 200 ml of water and 200 ml of ether (aqueous layer at pH 2). The aqueous layer was washed twice with 200 ml ether each time. The aqueous layer was adjusted to pH 11 with solid sodium hydroxide and extracted three times with 150 ml n-butanol each time. The butanol extract was dried over sodium sulfate, filtered and concentrated. The residue was taken up in tetrahydrofuran and filtered. The filtrate was evaporated to a syrup which was azeotroped with toluene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04754065 |
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| Quelldatensatz | uspto-grants-1988_06 |
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| ORD ID | ord-d093f0b609944700bdaaf51c8f8e4c0f |
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| Quellennotiz | uspto-grants-1988_06 |
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