반응식
[CH2:1]([O:3][C:4](=[O:17])[CH2:5][S:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1)(=[O:8])=[O:7])[CH3:2].[CH:18](Br)=[CH:19][C:20](=[CH2:22])[CH3:21].C1OCCOCCOCCOCCOCCOC1.C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[CH2:1]([O:3][C:4](=[O:17])[CH:5]([S:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1)(=[O:7])=[O:8])[CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])[CH3:2]참가 물질
6
실험 절차
To a stirred solution of (4-methoxy-benzenesulfonyl)-acetic acid ethyl ester (5.16 g, 20 mmol), isoprenyl bromide (3.0 g, 20 mmol) and 18-Crown-6 (500 mg) in acetone (250 ml) was added K2CO3 (10 gms, excess) and the mixture refluxed foe 24 hours. At the end, the reaction mixture was filtered and the acetone layer was concentrated. The residue obtained was extracted with chloroform, washed well with water, dried over anhydrous MgSO4, filtered and concentrated. The product obtained was purified by silica-gel column chromatography, eluting with 30% ethy acetate: hexane. The product 2-(4-methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester was isolated as a colourless oil. Yield: 3.0 g, 93%.
후처리
- temperaturethe mixture refluxed foe 24 hours
- filtrationAt the end, the reaction mixture was filtered
- concentrationthe acetone layer was concentrated
- customThe residue obtained
- extractionwas extracted with chloroform
- washwashed well with water
- dry with materialdried over anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe product obtained
- customwas purified by silica-gel column chromatography
- washeluting with 30% ethy acetate
출처 및 근거
- ORD 기록
- ord-38c567a749204ef4915213ea3d8356c1
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06172057B2
연결된 노트
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