反応式
[C:1]1([CH3:10])[C:2]([C:7]([OH:9])=[O:8])=[CH:3][CH:4]=[CH:5][CH:6]=1.[I:11]N1C(=O)CCC1=O>CN(C=O)C.O.CCOC(C)=O.CC([O-])=O.CC([O-])=O.[Pd+2]>[I:11][C:3]1[CH:4]=[CH:5][CH:6]=[C:1]([CH3:10])[C:2]=1[C:7]([OH:9])=[O:8]参加物
反応条件
- 温度
- 100 °C
実験手順
To a solution of o-toluic acid (2.00 g, 14.7 mmol) in dry DMF (60 mL) under an atmosphere of nitrogen was added N-iodosuccinimide (3.64 g, 16.2 mmol) followed by Pd(OAc)2 (0.330 g, 1.47 mmol). The resulting reaction mixture was heated to 100° C. and stirred for 17 hours. Upon cooling to room temperature the reaction was diluted with water (100 mL) and EtOAc (150 mL), the layers were separated and the aqueous layer was extracted with EtOAc (2×100 mL), the combined organics were washed with water (100 mL), brine (100 mL), water (100 mL), brine (100 mL), dried (MgSO4), filtered and concentrated in vacuo to give the title compound (I57) (3.56 g, 92% yield) as a brown oily solid; 1H NMR (400 MHz, CDCl3) δ 7.69 (d, J=7.9 Hz, 1H), 7.21 (d, J=7.6 Hz, 1H), 7.02 (t, J=7.8 Hz, 1H), 2.44 (s, 3H). LCMS Method C: rt 5.36 min.
後処理
- customThe resulting reaction mixture
- temperatureUpon cooling to room temperature the reaction
- customthe layers were separated
- extractionthe aqueous layer was extracted with EtOAc (2×100 mL)
- washthe combined organics were washed with water (100 mL), brine (100 mL), water (100 mL), brine (100 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-80277db792f34ba6893be86af00fb0ec
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US09012461B2
関連ノート
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