Aluminum isopropoxide → 2-(2,2,3-Trimethylcyclopent-3-en-1-yl)-2,4-dimethyl-4-pentenol
Reaktionsgleichung
CC(C)[O-].[Al+3].CC(C)[O-].CC(C)[O-].[CH3:14][C:15]([CH:22]1[CH2:26][CH:25]=[C:24]([CH3:27])[C:23]1([CH3:29])[CH3:28])([CH2:18][C:19]([CH3:21])=[CH2:20])[CH:16]=[O:17]>C(O)(C)C>[CH3:28][C:23]1([CH3:29])[C:24]([CH3:27])=[CH:25][CH2:26][CH:22]1[C:15]([CH3:14])([CH2:18][C:19]([CH3:21])=[CH2:20])[CH2:16][OH:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 4 neck 1 liter round bottomed flask was charged with 400 g of dry isopropanol and 100 g of aluminum isopropoxide (0.48 mole). The contents of the flask were refluxed (80° C.) and 200 g of 2,4-dimethyl-2-(2,2,3-trimethylcyclopent-3-en-1-yl)-4-pentenal at 95.2% (0.865 mole) were added dropwise under nitrogen over 80 minutes. The reaction was refluxed for 2 hours. Then the lights were distilled off to a pot temperature of 110° C. After cooling the batch was extracted with 150 ml of 10% sulfuric acid and 300 ml of hexane. The hexane extract was washed with 150 ml of water, 100 ml of 5% sodium carbonate, and 100 ml of brine. After drying with magnesium sulfate, the batch was filtered, concentrated in vacuo and the crude alcohol, 201.1 g, was distilled from 1 g of soda ash to afford 193.6 g of purified product (88% yield). BP 94° C./0.10 mmHg; 1H-NMR (300 MHz), δ1.007 (3H, s), 1.02 (3H, s), 1.42 (3H, s), 1.54 (3H, s), 1.83 (4H, br s), 2.0-2.4 (5H, br m), 3.60 (2H, AB quartet, JAB =11.1 Hz), 4.75 (1H, s), 4.88 (1H, s), 5.27 (1H, s); 13C-NMR (75 MHz), δ12.35, 20.07, 22.31, 25.48, 28.38, 30.96, 42.11, 45.10, 48.27, 54.77, 68.48, 114.81, 121.38, 144.22, 148.28; IR (Neat), 3400 br, 2980, 1040 cm-1 ; MS (m/e), 207 (M+ -15), 191, 109 (Base).