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Acetone → 5-Bromo-3-fluorobenzene-1,2-diamine

HRID 1521370
ノート
印刷プレビュー

反応式

HRID 1521370 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([F:12])[C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1.[NH4+].[Cl-].CC(C)=O>[Zn].O>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[C:4]([F:12])[CH:3]=1
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

6

反応物 3

HCID 180AcetoneHCID 25517Ammonium ChlorideHCID 669372325-Bromo-3-fluoro-2-nitroaniline

生成物 1

HCID 27732795-Bromo-3-fluorobenzene-1,2-diamine

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 962Water溶媒

反応条件

温度
23 °C

実験手順

To a solution of 5-bromo-3-fluoro-2-nitro-phenylamine (2 g, 8.5 mmol), NH4Cl (6.81 g, 127.6 mmol), acetone (100 mL) and water (20 mL), was added zinc powder portion-wise (three equal portions over 5 minutes) (8.34 g, 127.6 mmol) at 0° C. The mixture was stirred for 2 h then warmed to 23° C. The mixture was filtered through Celite® and the solvents were concentrated under reduced pressure. The mixture was re-dissolved in EtOAc/DCM and filtered a second time through Celite® and the solvents were evaporated. The crude mixture was diluted with EtOAc (200 mL), washed with brine (40 mL), dried, filtered, and concentrated under reduced pressure. The resultant residue was used in the next reaction without further purification.

後処理

  1. filtrationThe mixture was filtered through Celite®
  2. concentrationthe solvents were concentrated under reduced pressure
  3. dissolutionThe mixture was re-dissolved in EtOAc/DCM
  4. filtrationfiltered a second time through Celite®
  5. customthe solvents were evaporated
  6. additionThe crude mixture was diluted with EtOAc (200 mL)
  7. washwashed with brine (40 mL)
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe resultant residue was used in the next reaction without further purification

出典と根拠

ORDレコード
ord-65461e0319ce4088a4d70236553c50c4
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073923B2

反応ノート

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