Water → 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one
반응식
F[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]2.[C:13]1([SH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+].O>CN1C(=O)CCC1.CCOC(C)=O>[C:13]1([S:19][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]3)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
A solution of 6-fluoro-3,4-dihydro-2H-naphthalen-1-one (5.51 g, 33.56 mmol), benzenethiol (4.07 g, 3.79 mL, 36.92 mmol) and K2CO3 (9.28 g, 67.12 mmol) in 50 mL of N-methyl pyrrolidinone (NMP) was heated to 80° C. under argon and stirred at 80° C. for 2 hours. The reaction mixture was poured into 500 mL of water and diluted with 300 mL of EtOAc. The layers were separated and the aqueous layer was extracted twice with 250 mL of EtOAc. The combined organic layers were washed with water, saturated brine, and then dried over MgSO4. The solvent was removed under reduced pressure to yield an oil which was eluted through silica gel using hexanes/EtOAc (9:1). Removal of solvent under reduced pressure provided 8.05 g (31.65 mmol, 94.31%) of 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one as a pale yellow oil. MS: 255 (M+H)+.
후처리
- customThe layers were separated
- extractionthe aqueous layer was extracted twice with 250 mL of EtOAc
- washThe combined organic layers were washed with water, saturated brine
- dry with materialdried over MgSO4
- customThe solvent was removed under reduced pressure
- customto yield an oil which
- washwas eluted through silica gel
- customRemoval of solvent under reduced pressure
출처 및 근거
- ORD 기록
- ord-f313669e91084be78c0365b7cc48a292
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889906B2
반응 노트
불러오는 중…