反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:12][OH:13])[CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[OH-].[Na+]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([C:8]([F:9])([F:10])[F:11])[CH:7]=1)[CH:12]=[O:13]参加物
反応条件
- 温度
- 0 °C
実験手順
A solution of [3-bromo-5-(trifluoromethyl)phenyl]methanol (409 mg, 1.61 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. and then Dess-Martin periodinane (1.02 g, 2.41 mmol) was added. The reaction was stirred at 0° C. for 30 minutes and then warmed to room temperature. After stirring at room temperature for thirty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (100 mL), and the organic extracts were washed with 1N NaOH (25 mL), then brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 25% EtOAc/hexanes afforded 3-bromo-5-(trifluoromethyl)benzaldehyde. Rf=0.60 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 8.20 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H).
後処理
- temperaturewarmed to room temperature
- stirringAfter stirring at room temperature for thirty minutes
- extractionThe mixture was extracted with EtOAc (100 mL)
- washthe organic extracts were washed with 1N NaOH (25 mL)
- dry with materialbrine (25 mL), dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customPurification by flash chromatography with 25% EtOAc/hexanes
出典と根拠
- ORDレコード
- ord-c8db1d8fd8d745c88b07a88109cc08e0
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193365B2
関連ノート
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