반응식
[CH3:1][C:2]1([CH3:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([CH3:12])([CH3:11])[CH:3]1[CH3:13].[CH3:15]C1(C)C2C(CCCC2)C(C)(C)C1C.Cl.[OH-:30].[Na+]>>[CH3:11][C:4]1([CH3:12])[C:5]2[CH2:6][CH2:7][CH2:8][CH:9]([CH:15]=[O:30])[C:10]=2[C:2]([CH3:14])([CH3:1])[CH:3]1[CH3:13]참가 물질
5
실험 절차
prepared according to the disclosure of U.S. Pat. No. 4,902,840 issued on Feb. 20, 1990, the specification for which is incorporated herein by reference; 20% 1,1,2,3,3-pentamethylindane and 35% hexahydro-1,1,2,3,3-pentamethylindane is heated to 150° C. Hydrogen chloride gas evolves and is passed through a caustic soda scrubber. This solution is then washed with a 5% aqueous sodium hydroxide solution, dried over anhydrous magnesium sulfate and used without further purification in the next step, the carrying out of an oxo-reaction.
후처리
- customprepared
- washThis solution is then washed with a 5% aqueous sodium hydroxide solution
- dry with materialdried over anhydrous magnesium sulfate
- customused without further purification in the next step
- customthe carrying out of an oxo-reaction
출처 및 근거
- ORD 기록
- ord-0c5e48e985044412bfd33fa090a3cb16
- 출처 데이터셋
- uspto-grants-2001_08
- 특허 번호
- US06271193B1
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