Triethylamine → HCID 66572312, Verbindung
Reaktionsgleichung
[CH2:1]([O:8][C:9]1[CH:18]=[CH:17][C:12](/[C:13](/Cl)=[N:14]\[OH:15])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCN(CC)CC.[C:26]([O:30][CH2:31][CH3:32])(=[O:29])[C:27]#[CH:28]>C1(C)C=CC=CC=1.C(OCC)(=O)C>[CH2:1]([O:8][C:9]1[CH:18]=[CH:17][C:12]([C:13]2[CH:28]=[C:27]([C:26]([O:30][CH2:31][CH3:32])=[O:29])[O:15][N:14]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
To (E)-4-(benzyloxy)-N-hydroxybenzimidoyl chloride (7.8 g) in Toluene (78 ml), Ethyl propiolate (7.25 ml) was added and stirred. To this, Et3N (4.58 ml) was added dropwise since reaction was exothermic and the reaction mixture was then heated to 80° C. for 2 hours. The reaction mixture was cooled, diluted with Ethyl acetate and washed successively with 0.1M Aqueous HCl, water and brine. Organic layer was collected and concentrated to obtain dark brown residue which was purified by column chromatography (silica gel, DCM) to obtain pale brown solid which was crystallized from DCM-Petroleum ether to obtain the title compound as off white solid. Yield: 2.83 g (29%); MS (ES+): m/z 324 (M+1); 1HNMR (CDCl3; 300 MHz): δ 7.8 (d, 2H), 7.36-7.47 (m, 5H), 7.28 (s, 1H), 7.1 (d, 2H), 5.14 (s, 2H), 4.48 (q, 2H), 1.45 (t, 3H).
Aufarbeitung
- temperatureThe reaction mixture was cooled
- washwashed successively with 0.1M Aqueous HCl, water and brine
- customOrganic layer was collected
- concentrationconcentrated
- customto obtain dark brown residue which
- customwas purified by column chromatography (silica gel, DCM)
- customto obtain pale brown solid which
- customwas crystallized from DCM-Petroleum ether
Quellen und Nachweise
- ORD-Eintrag
- ord-5737acb0d24146cf97b0b0a78c91f7c5
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08835428B2
Notizen zur Reaktion
Wird geladen…