Water → 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one
反応式
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>CN1CCCC1=O.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]=1参加物
反応条件
- 温度
- 80 °C
実験手順
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-methylpyrrolidinone (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)+.
後処理
- 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
出典と根拠
- ORDレコード
- ord-605a42c583b14946b6e591331f7429f8
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08093424B2
反応ノート
読み込み中…