반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([C:13](=[O:16])[CH2:14][CH3:15])[CH:7]=[CH:6]2.[CH3:17][O:18][C:19](=[O:28])[C@@H:20]([C@H:22]([C:24]([O:26][CH3:27])=[O:25])O)[OH:21].C(OC)(OC)OC.CS(O)(=O)=O>C([O-])([O-])=O.[Na+].[Na+]>[CH3:27][O:26][C:24]([C@H:22]1[C@H:20]([C:19]([O:18][CH3:17])=[O:28])[O:21][C:13]([CH2:14][CH3:15])([C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH:4]=3)[CH:9]=2)[O:16]1)=[O:25]참가 물질
실험 절차
1-(6-methoxy-2-naphthyl)-propan-1-one (46.5 g; 0.217 moles), L(+)tartaric acid dimethyl ester (300 g), trimethyl orthoformate (94 g; 0.887 moles) are gradually heated up to complete solution. Methanesulphonic acid (1.48 g; 0.0154 moles) is then added and the obtained solution is refluxed for 2 hours; it is cooled at room temperature and the reaction mixture is slowly added to a 10% solution of Na2CO3 (500 ml). It is extracted with methylene chloride and the organic extracts are repeatedly washed with water. The organic phase is dried on Na2SO4 and the solvent is evaporated under reduced pressure. The residue is crystallized from methanol (250 ml). The desired product is obtained (51.68 g; 0.138 moles; yield 63.6%) having the following characteristics:
후처리
- temperaturethe obtained solution is refluxed for 2 hours
- extractionIt is extracted with methylene chloride
- washthe organic extracts are repeatedly washed with water
- customThe organic phase is dried on Na2SO4
- customthe solvent is evaporated under reduced pressure
- customThe residue is crystallized from methanol (250 ml)
출처 및 근거
- ORD 기록
- ord-099d9cd077d147df8cd7752129a246e3
- 출처 데이터셋
- uspto-grants-1989_03
- 특허 번호
- US04810819
연결된 노트
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