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Bromine → 1-Bromo-4-methoxy-2,5-dimethylbenzene

HRID 990165
ノート
印刷プレビュー

反応式

HRID 990165 の反応式
[Br:1]Br.[CH3:3][C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[CH:6][C:5]=1[O:11][CH3:12]>[Fe]>[Br:1][C:8]1[C:7]([CH3:10])=[CH:6][C:5]([O:11][CH3:12])=[C:4]([CH3:3])[CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408Bromine2 回HCID 743502,5-Dimethylanisole

生成物 1

HCID 27525981-Bromo-4-methoxy-2,5-dimethylbenzene

試薬・触媒・溶媒 1

HCID 23925Iron触媒

実験手順

Bromine (291.5 g, 1835 mmol) was added dropwise while stirring to an initially charged mixture of 2,5-dimethylanisole (250 g, 1835 mmol) and Fe powder (3.25 g). The commencement of the reaction could be recognized by gas evolution. The remaining bromine was then added dropwise at room temperature over a period of 30-40 minutes while cooling on a water bath. The reaction mixture was stirred further for about 4 hours. The solution was then separated from the Fe powder, a little chloroform was added and the mixture was shaken with water, which led to the solution becoming lighter in color. After shaking with 50 ml of saturated aqueous Na2SO3 solution, the solution had become completely decolorized. It was then shaken again with dilute aqueous NaOH and twice with H2O and, after drying, the solvent was taken off. The crude product was fractionally distilled under reduced pressure.

後処理

  1. customThe commencement of the reaction
  2. temperaturewhile cooling on a water bath
  3. customThe solution was then separated from the Fe powder
  4. additiona little chloroform was added
  5. stirringthe mixture was shaken with water, which
  6. stirringAfter shaking with 50 ml of saturated aqueous Na2SO3 solution
  7. stirringIt was then shaken again with dilute aqueous NaOH and twice with H2O
  8. customafter drying
  9. distillationThe crude product was fractionally distilled under reduced pressure

出典と根拠

ORDレコード
ord-9ebe641e394c414ba8add6e934ceb603
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06458909B1

反応ノート

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