Hydrochloric Acid → 3-methylthio-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one
반응식
S([O-])([O-])=O.[Na+].[Na+].N[C:8]1[CH:19]=[CH:18][C:11]2[CH2:12][CH2:13][CH2:14][CH2:15][C:16](=[O:17])[C:10]=2[CH:9]=1.Cl.O.O.O.C([O-])(=O)C.[Na+].[CH3:29][S-:30].[Na+].[OH-].[Na+]>O>[CH3:29][S:30][C:8]1[CH:19]=[CH:18][C:11]2[CH2:12][CH2:13][CH2:14][CH2:15][C:16](=[O:17])[C:10]=2[CH:9]=1참가 물질
반응물 6
생성물 1
시약·촉매·용매 1
실험 절차
A solution of sodium sulfite (3.31 g, 47.94 mmol) in water (5 ml) was added dropwise to a mixture of 3-amino-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one (8.00 g, 45.65 mmol) and 35% hydrochloric acid (20 ml) under ice-cooling and stirred under ice-cooling for 20 minutes. Sodium acetate trihydrate (33 g) was added to the reaction mixture and the resulting mixture was added dropwise to a 15% aqueous sodium thiomethoxide solution (42.67 g, 91.31 mmol). The reaction mixture was stirred at 80° C. for 1.5 hours, adjusted to pH 9 with an aqueous sodium hydroxide solution and then extracted with ethyl acetate. The extract solution was washed with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/30) to obtain 4.33 g of 3-methylthio-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one.
후처리
- temperaturecooling
- temperaturecooling for 20 minutes
- stirringThe reaction mixture was stirred at 80° C. for 1.5 hours
- extractionextracted with ethyl acetate
- washThe extract solution was washed with water
- dry with materiala saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/30)
출처 및 근거
- ORD 기록
- ord-7d4000496e0c473ab6affa1d0ce2216d
- 출처 데이터셋
- uspto-grants-2002_04
- 특허 번호
- US06369110B1
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