反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9]O)=[CH:4][CH:3]=1.P(Br)(Br)[Br:12]>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][Br:12])=[CH:4][CH:3]=1参加物
4
実験手順
To a solution of 2-(4-fluorophenyl)ethyl alcohol (13.4 mL, 107 mmol) in dry toluene (150 mL) at 0° C. was added phosphorous tribromide (21.1 mL, 224 mmol). The resulting mixture was stirred at ambient temperature for 5 days and then recooled to 0° C. and crushed ice (200 g) added. The aqueous layer was extracted with ether (2×120 mL) and the combined organic extracts were then washed with saturated aqueous sodium bicarbonate solution (2×30 mL), dried (MgSO4) and concentrated in vacuum. Distillation afforded 2-(4-fluorophenyl)ethyl bromide as a colorless oil (14.08 g, 31%); b.p. 103° C. @12 mm Hg.
後処理
- customrecooled to 0° C.
- additionadded
- extractionThe aqueous layer was extracted with ether (2×120 mL)
- washthe combined organic extracts were then washed with saturated aqueous sodium bicarbonate solution (2×30 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuum
- distillationDistillation
出典と根拠
- ORDレコード
- ord-78f2978710bb4377b00338b675d641f6
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06713627B2
関連ノート
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