HCID 21751901, Verbindung → HCID 68780289, Verbindung
Reaktionsgleichung
[CH2:1]([CH:3]([NH:8][NH2:9])[C:4]([CH3:7])([CH3:6])[CH3:5])[CH3:2].FC1C([O:17][C:18]([C:20]2[CH:38]=[CH:37][C:23]3[O:24][CH2:25][C@@H:26]([C:28](C)(C)[O:29][SiH2]C(C)(C)C)[O:27][C:22]=3[C:21]=2[CH3:39])=O)=C(F)C(F)=C(F)C=1F>C(OCC)(=O)C>[CH2:1]([CH:3]([NH:8][NH:9][C:18]([C:20]1[CH:38]=[CH:37][C:23]2[O:24][CH2:25][C@H:26]([CH2:28][OH:29])[O:27][C:22]=2[C:21]=1[CH3:39])=[O:17])[C:4]([CH3:7])([CH3:6])[CH3:5])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To the biphasic preparation of (1-ethyl-2,2-dimethyl-propyl)-hydrazine described above, was added a solution of approximately one gram 3(S)-(tert-butyl-dimethyl-silanyloxymethyl)-5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid pentafluorophenyl ester dissolved in 10 mL ethyl acetate. The mixture was stirred at room temperature for 2 hours, after which time the aqueous phase was withdrawn and replaced with 1 M K2CO3. The mixture was stirred overnight. The aqueous layer was separated off, and the organic layer was extracted once with 1 M K2CO3 and then once with water. The organic phase was dried. The crude product was chromatographed on silica gel using a step gradient of 10% ether in hexane followed by neat ether, yielding 3(S)-hydroxymethyl-5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid N′-(1-ethyl-2,2-dimethyl-propyl)-hydrazide. 1H NMR (500 MHz, CDCl3) δ (ppm): 7.15 (br, 1H), 6.85 (d, 1H), 6.73 (d, 1H), 4.85 (br, 1H), 4.3 (d, 1H), 4.25 (m, 1H), 4.1 (dd, 1H), 3.87 (m, 2H), 2.41 (m, 1H), 2.29 (s, 3H), 1.8 (br, 1H); 1.65 (m, 1H), 1.3 (m, 1H), 1.45 (t, 3H), 0.98 (s, 9H); TLC: Rf=0.23 (1:1 ethyl acetate:hexane).