Dichloromethane → HCID 59627740、化合物
反応式
B(Br)(Br)Br.C[O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([OH:16])=[O:15])=[CH:9][C:8]=1[C:17]([F:20])([F:19])[F:18].Cl[CH2:22]Cl>>[OH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([O:16][CH3:22])=[O:15])=[CH:9][C:8]=1[C:17]([F:20])([F:19])[F:18]参加物
実験手順
Boron tribromide (8.02 mL, 84.87 mmol) was added dropwise to 2-(4-methoxy-3-(trifluoromethyl)phenyl)acetic acid (3.31 g, 14.13 mmol) in dichloromethane (250 mL) while maintaining the temperature below 10° C. After complete addition the reaction mixture was removed from the ice bath and allowed to stir at ambient temperature under nitrogen for 90 minutes. The reaction mixture was added dropwise to ice cold methanol (150 mL) and the mixture was stirred at ambient temperature for a further 40 minutes. The reaction mixture was evaporated to afford to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford methyl 2-(4-hydroxy-3-(trifluoromethyl)phenyl)acetate (1.100 g, 33.2%) as a pale yellow oil.
後処理
- temperaturewhile maintaining the temperature below 10° C
- additionAfter complete addition the reaction mixture
- customwas removed from the ice bath
- additionThe reaction mixture was added dropwise to ice cold methanol (150 mL)
- stirringthe mixture was stirred at ambient temperature for a further 40 minutes
- customThe reaction mixture was evaporated
- customto afford
- customto afford crude product
- customThe crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane
- customPure fractions were evaporated to dryness
出典と根拠
- ORDレコード
- ord-60e1409951054af4b8a53644b65967fe
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08188092B2
反応ノート
読み込み中…