反応式
[Br:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](O)=[O:6]>C1COCC1>[Br:1][C:2]1[C:3]([CH3:11])=[C:4]([CH2:5][OH:6])[CH:8]=[CH:9][CH:10]=1参加物
3
実験手順
To a solution of 3-bromo-2-methyl benzoic acid (35 g, 160 mmol) in THF (200 mL) was added borane THF complex (1.0 M, 210 mL, 210 mmol). The mixture was allowed to stir for 24 hours. The reaction was quenched with water. The solvent THF was removed under reduced pressure. The resulting solid was dissolved in ethyl acetate (500 mL), washed with 1N hydrochloric acid, saturated sodium bicarbonate, and brine. The combined organic layers were dried over sodium sulfate and concentrated to afford (3-bromo-2-methylphenyl)methanol.
後処理
- customThe reaction was quenched with water
- customThe solvent THF was removed under reduced pressure
- dissolutionThe resulting solid was dissolved in ethyl acetate (500 mL)
- washwashed with 1N hydrochloric acid, saturated sodium bicarbonate, and brine
- dry with materialThe combined organic layers were dried over sodium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-f78fa7cad65f4569865267fde3203bcf
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09108947B2
関連ノート
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