HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1393615Erstellt: 27. Oktober 2026
Benzyl Alcohol → 6-(Phenylmethoxy)-9H-purin-2-amine
https://huagongshe.com/reaction/1393615
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Alcohol | HCID 244 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Amino-6-chloropurine | HCID 5360349 | — |
| Lösungsmittel | tert-Butyl methyl ether | HCID 15413 | — |
| Produkt | 6-(Phenylmethoxy)-9H-purin-2-amine | HCID 4578 | 92% |
Reaktionsschritte
Benzyl alcohol (37.5 g, 0.347 mol) and sodium hydroxide (2.96 g, 0.074 mol) were mixed and heated, and sodium hydroxide was dissolved. After cooling, 2-amino-6-chloropurine (6.00 g, 0.035 mol) was added, and the reaction was completed by heating and stirring at 80-90° C. for 5 hr. Methyl tert-butyl ether (120 ml) was added to the reaction mixture, and the mixture was extracted twice with 1% aqueous sodium hydroxide solution (70 ml). The obtained aqueous alkali layers were combined, washed with toluene, and after removing toluene, neutralized with 35% hydrochloric acid to pH 6-8. The precipitated crystals were collected by filtration. The obtained crystals were dried under reduced pressure to give 2-amino-6-benzyloxypurine (7.60 g, 0.032 mol, yield 92%) as crude crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07345170B2 |
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| Quelldatensatz | uspto-grants-2008_03 |
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| ORD ID | ord-e3d0d0b9e5c44006a966ed6407134047 |
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| Quellennotiz | uspto-grants-2008_03 |
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