HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2395039Erstellt: 23. Oktober 2026
tert-Butanol → t-Butyloxycarbonyl-4-{3-(2-benzyloxyphenyl)propyl]benzene-amine
https://huagongshe.com/de/reaction/2395039
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | 4-(3-(2-Benzyloxyphenyl)propyl]benzoic acid | HCID 18973764 | — |
| Produkt | t-Butyloxycarbonyl-4-{3-(2-benzyloxyphenyl)propyl]benzene-amine | HCID 18973826 | — |
Reaktionsschritte
A mixture of 4-[3-(2-benzyloxyphenyl)propyl]benzene carboxylic acid (8.39 g), diphenylphosphoryl azide (5.74 ml) and triethylamine (7.1 ml) in t-butanol (80 ml) was heated under reflux in an argon atmosphere for 16 hours. The reaction mixture was evaporated to dryness and the residue partitoned between ethyl acetate and water. The ethyl acetate extract was washed once each with 2N HCl, water, saturated aqueous sodium bicarbonate solution and brine (20 ml each time) and dried (MgSO4). The solvent was evaporated and the residue subjected to flash chromatography eluted with a mixture of dichloromethane:hexane (1:1 v/v) to give N t-butyloxycarbonyl-4-{3-(2-benzyloxyphenyl)propyl]benzene-amine 7.69 g m.p. 86°-8° C. which was used directly in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05811459 |
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| Quelldatensatz | uspto-grants-1998_09 |
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| ORD ID | ord-28b7cf6826bf4a3c962538dcb0786d6e |
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| Quellennotiz | uspto-grants-1998_09 |
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