Reaktionsgleichung
[NH2:1][CH2:2][C:3]#[CH:4].C(N(CC)CC)C.[O:12]([C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22](Cl)=[O:23])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>ClCCl>[O:12]([C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22]([NH:1][CH2:2][C:3]#[CH:4])=[O:23])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a dichloromethane (25 mL) solution of amino-2-propyne (0.96 g, 17.43 mmol) and triethylamine (3.33 mL, 23.7 mmol) at 0° C. was added 3-phenoxybenzoyl chloride (3.68 g, 15.8 mmol) in dichloromethane (25 mL) in a dropwise fashion. The reaction was stirred for 1 h after removing the cooling bath and partitioned between dichloromethane and 10% aqueous HCl. The layers were separated and the aqueous layer was extracted with dichloromethane (2×). The combined organic layers were washed (1×, saturated sodium bicarbonate; 1×, brine), dried (MgSO4), and concentrated under vacuum to give a golden oil. Recrystallization with ehter ethyl acetate provided the title compound as a colorless solid (2.95 g, 74%).
Aufarbeitung
- customafter removing the cooling bath
- custompartitioned between dichloromethane and 10% aqueous HCl
- customThe layers were separated
- extractionthe aqueous layer was extracted with dichloromethane (2×)
- washThe combined organic layers were washed (1×, saturated sodium bicarbonate; 1×, brine)
- dry with materialdried (MgSO4)
- concentrationconcentrated under vacuum
- customto give a golden oil
- customRecrystallization with ehter ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-9b6da40b4f8d4c4587842a6f30a4effb
- Quelldatensatz
- uspto-grants-1996_05
- Patentnummer
- US05514702
Verknüpfte Notizen
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