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Sodium Hydroxide → 1-Bromo-4-methoxy-2,5-dimethylbenzene

HRID 988932
ノート
印刷プレビュー

反応式

HRID 988932 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].[O-]S([O-])=O.[Na+].[Na+].[OH-].[Na+]>[Fe].O>[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

7

反応物 4

HCID 14798Sodium HydroxideHCID 24408Bromine2 回HCID 24437Sodium SulfiteHCID 743502,5-Dimethylanisole

生成物 1

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

試薬・触媒・溶媒 2

HCID 23925Iron触媒
HCID 962
Water
溶媒

実験手順

Bromine (291.5 g, 1835 mmol) was added dropwise with stirring to an initially introduced mixture of 2,5-dimethylanisole (250 g, 1835 mmol) and Fe powder (3.25 g). The commencement of the reaction was evident from gas evolution. The remainder of the bromine was subsequently added dropwise over the course of 30-40 minutes at room temperature with water-bath cooling. The reaction mixture was stirred for about a further 4 hours. The Fe powder was subsequently separated off, a little chloroform was added to the solution, and the solution was washed by shaking with water, resulting in the solution becoming paler. After the solution had been shaken with 50 ml of saturated aqueous Na2SO3 solution, it had become completely colorless. The solution was shaken again with dilute aqueous NaOH and twice with H2O and dried, and the solvent was stripped off. The crude product was subjected to fractional distillation under reduced pressure.

後処理

  1. temperaturecooling
  2. customThe Fe powder was subsequently separated off
  3. additiona little chloroform was added to the solution
  4. washthe solution was washed
  5. stirringby shaking with water
  6. customresulting in the solution
  7. customdried
  8. distillationThe crude product was subjected to fractional distillation under reduced pressure

出典と根拠

ORDレコード
ord-323c195262c74069b9b23f36350f7345
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06638646B2

反応ノート

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