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Ammonium Chloride → 5-Bromo-3-fluorobenzene-1,2-diamine

HRID 1429212
ノート
印刷プレビュー

反応式

HRID 1429212 の反応式
[Br:1][C:2]1[CH:8]=[C:7]([N+:9]([O-])=O)[C:5]([NH2:6])=[C:4]([F:12])[CH:3]=1.[Cl-].[NH4+]>C1COCC1.CCO.O.[Fe]>[Br:1][C:2]1[CH:8]=[C:7]([NH2:9])[C:5]([NH2:6])=[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

7

反応物 2

HCID 25517Ammonium ChlorideHCID 27733814-Bromo-2-fluoro-6-nitroaniline

生成物 1

HCID 27732795-Bromo-3-fluorobenzene-1,2-diamine収率 99.9%

試薬・触媒・溶媒 4

HCID 23925Iron触媒HCID 702Ethanol溶媒HCID 962Water溶媒
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
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
95 °C

実験手順

To a solution of 4-bromo-2-fluoro-6-nitroaniline (0.5 g, 2.1 mmol) in THF (4.6 mL), EtOH (4.6 mL) and H2O (1.5 mL) was added iron powder (0.6 g, 10.6 mmol) and ammonium chloride (0.17 g, 3.2 mmol). The resulting mixture was stirred at 95° C. for 22 hours. The mixture was cooled to room temperature and filtered through diatomaceous earth. The solid was washed with EtOH until no further color came through the filter. The filtrate was concentrated and the residue was dissolved in EtOAc, washed with H2O and brine, dried over Na2SO4, filtered and concentrated to give the title compound (0.43 g, 99%) as a brown, waxy solid.

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through diatomaceous earth
  3. washThe solid was washed with EtOH until no further color
  4. concentrationThe filtrate was concentrated
  5. dissolutionthe residue was dissolved in EtOAc
  6. washwashed with H2O and brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-ed75b82571c449889bc03bf5d4ffd4ec
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08937150B2

反応ノート

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