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Sodium Sulfite → 2-Bromo-4-chloro-5-methoxyaniline

HRID 705369
ノート
印刷プレビュー

反応式

HRID 705369 の反応式
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[O:9][CH3:10].[Br:11]N1C(=O)CCC1=O.[O-]S([O-])=O.[Na+].[Na+]>C(Cl)Cl>[Br:11][C:7]1[CH:8]=[C:2]([Cl:1])[C:3]([O:9][CH3:10])=[CH:4][C:5]=1[NH2:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24437Sodium SulfiteHCID 67184N-bromobutanimideHCID 131036924-Chloro-3-methoxyaniline

生成物 1

HCID 147747832-Bromo-4-chloro-5-methoxyaniline収率 80%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
20 °C

実験手順

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

A solution of 4-chloro-3-methoxyaniline (1.0 equivalent) dissolved in CH2Cl2 (15 volumes) at 5° C. was treated portion wise with N-bromosuccinimide (1.03 equivalents), warmed to 20° C. and mixed for 5 minutes. A 5% aqueous Na2SO3 solution (10 volumes) was added and the mixture was stirred for 10 minutes. The layers were separated and the organic layer was washed with water and saturated brine, dried (Na2SO4), filtered and concentrated. The resulting solid was triturated with a minimal volume of heptane and the solid was collected by filtration and dried to constant mass (80% yield).

後処理

  1. additionmixed for 5 minutes
  2. customThe layers were separated
  3. washthe organic layer was washed with water and saturated brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe resulting solid was triturated with a minimal volume of heptane
  8. filtrationthe solid was collected by filtration
  9. customdried to constant mass (80% yield)

出典と根拠

ORDレコード
ord-58383cd619f7474585f0ed824f65dcf6
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09173887B2

反応ノート

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