Benzoyl Peroxide → 2-Bromo-1-(bromomethyl)-4-fluorobenzene
反応式
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH3:9].[Br:10]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][Br:10]参加物
5
実験手順
A mixture of 18.9 g (100 mmol) of 2-bromo-4-fluorotoluene, 17.8 g (100 mmol) of N-bromosuccinimide, 400 mg of benzoyl peroxide, and 200 ml of CCl4 were refluxed for 2 h. The reaction mixture was filtered through a glass frit (G2), and the precipitate was additionally washed with 3×50 ml of CCl4. The combined filtrate was evaporated to dryness. Fractional distillation of the residue (bp 92-96° C./4 mm Hg) gave the title product as colorless oil. Yield 20.4 g (76%).
後処理
- temperaturewere refluxed for 2 h
- filtrationThe reaction mixture was filtered through a glass frit (G2)
- washthe precipitate was additionally washed with 3×50 ml of CCl4
- customThe combined filtrate was evaporated to dryness
- distillationFractional distillation of the residue (bp 92-96° C./4 mm Hg)
出典と根拠
- ORDレコード
- ord-94c9944c3f9d407eabf4c54ef871c94b
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07446216B2
反応ノート
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