반응식
[CH2:1]([C:3]([OH:18])([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=1)[C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH3:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH2:32]Cl)[N:27]=1>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.C(OCC)(=O)C>[CH3:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH2:32][O:10][C:7]2[CH:6]=[CH:5][C:4]([C:3]([C:11]3[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=3)([OH:18])[CH2:1][CH3:2])=[CH:9][CH:8]=2)[N:27]=1참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
13.1 g. of α-ethyl-α-(4-chlorophenyl)-4-hydroxybenzyl-alcohol, 14 g. of anhydrous potassium carbonate, 0.85 g. of tetrabutylammonium hydrogensulfate and 7.8 g. of 2-methyl-6-chloromethyl-pyridine in 140 ml. of ethyl acetate are boiled for 18 hours. The solvent is distilled off under reduced pressure, to the residue water is added, and it is extracted with ether. The ethereal solution is washed to neutral with a 5% aqueous potassium hydroxide solution and subsequently water, dried over anhydrous magnesium sulfate, and evaporated in vacuo. Crystallization of the residue from a mixture of hexane and ethyl acetate yields 13.6 g. of the title compound, melting at 100° to 101° C.
후처리
- distillationThe solvent is distilled off under reduced pressure, to the residue water
- additionis added
- extractionit is extracted with ether
- washThe ethereal solution is washed to neutral with a 5% aqueous potassium hydroxide solution and subsequently water
- dry with materialdried over anhydrous magnesium sulfate
- customevaporated in vacuo
- customCrystallization of the residue
- additionfrom a mixture of hexane and ethyl acetate
- customyields 13.6 g
출처 및 근거
- ORD 기록
- ord-2be7deb7c5794779bbdbc1444ceead4d
- 출처 데이터셋
- uspto-grants-1986_07
- 특허 번호
- US04598080
연결된 노트
불러오는 중…