반응식
C([Mg]Br)C.[Cl:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[CH:12]=[C:11]([SH:16])[CH:10]=[CH:9]2.[O:17]1[CH2:19][C@@H:18]1[C:20]([O:22][CH3:23])=[O:21].[Cl-].[NH4+]>C(OCC)C.C1COCC1>[Cl:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[CH:12]=[C:11]([S:16][CH2:19][C@@H:18]([OH:17])[C:20]([O:22][CH3:23])=[O:21])[CH:10]=[CH:9]2참가 물질
실험 절차
Under argon atmosphere, a 3 M solution of ethylmagnesium bromide in diethyl ether was added dropwise to THF (25 mL) with ice cooling. To this solution, a solution of 6-chloronaphthalene-2-thiol (5.0 g) in THF (50 mL) was added dropwise at 0C, and the mixture was mixed at room temperature for 30 minutes. To this solution, a solution of methyl (2R)-oxirane-2-carboxylate (2.3 mL) in THF (15 mL) was added dropwise, and the reaction solution was mixed at room temperature for 3 hours. To the reaction solution, an aqueous ammonium chloride solution (50 mL) was added, and the mixture was extracted with ethyl acetate (100 mL). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was recrystallized from hexane/ethyl acetate (3:1) to give the title compound (5.9 g, 77%) as colorless needle-shaped crystals.
후처리
- additionthe mixture was mixed at room temperature for 30 minutes
- additionthe reaction solution was mixed at room temperature for 3 hours
- extractionthe mixture was extracted with ethyl acetate (100 mL)
- washThe extract was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was recrystallized from hexane/ethyl acetate (3:1)
출처 및 근거
- ORD 기록
- ord-7fed1efc7429455cb84ab502c144dc5c
- 출처 데이터셋
- uspto-grants-2009_05
- 특허 번호
- US07534887B2
연결된 노트
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