Hydrochloric Acid → HCID 19857690、化合物
反応式
BrBr.Cl.[CH3:4][C:5]1[CH:10]=[CH:9][CH2:8][C:7]([CH3:12])([CH3:11])[C:6]=1[CH2:13][CH2:14][C:15](=[O:17])[CH3:16]>C(Cl)(Cl)Cl>[CH3:11][C:7]1([CH3:12])[CH:6]([CH2:13][CH2:14][C:15](=[O:17])[CH3:16])[C:5](=[CH2:4])[CH:10]=[CH:9][CH2:8]1参加物
5
実験手順
The resulting mixture is cooled in an ice-sodium chloride bath and a mixture of 3.2 grams of bromine and 9 ml chloroform is added drop-wise with stirring over a half hour period. The reaction mass is then stirred at 5°C for a period of 5 hours and then concentrated under reduced pressure. The resulting residue is then heated on a steam bath for a period of 3 hours after 11 ml of N,N-Diethyl-aniline has been added to the residue. After 3 hours 2.5 ml pyridine is then added to the reaction mass and heating is continued for 1/2 hour longer. To the cooled reaction mixture are added 50 ml of 5 N Hydrochloric acid. The aqueous layer is then extracted with three 100 ml portions of n-pentane. The combined pentane extracts are washed with two 50 ml portions of 5 N hydrochloric acid, then two 50 ml 10% sodium bicarbonate solution portions and two 100 ml portions of distilled water. The pentane extracts are then evaporated after drying over anhydrous sodium sulfate yielding (confirmed by infrared and mass spectral analysis) a mixture containing 90% 4-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-2-butanone and 10% 4-(6,6-dimethyl-2-methylene-3-cyclohexen-1-yl)-2-butanone (over-all yield: 8.8%). The 90:10 mixture of 4-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-2-butanone and 4-(6,6-dimethyl-2-methylene-3-cyclohexen-1-yl)-2-butanone distills at 65°C and at 15 mm Hg. pressure.