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Ammonium Chloride → 3-[(Dimethylamino)methyl]-4-fluoroaniline

HRID 1257266
ノート
印刷プレビュー

反応式

HRID 1257266 の反応式
[NH4+].[Cl-].[F:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[CH:6][C:5]=1[CH2:13][N:14]([CH3:16])[CH3:15]>CCO.[Fe]>[CH3:16][N:14]([CH2:13][C:5]1[CH:6]=[C:7]([CH:8]=[CH:9][C:4]=1[F:3])[NH2:10])[CH3:15]
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 2

HCID 25517Ammonium ChlorideHCID 58998500HCID 58998500、化合物

生成物 1

HCID 450889853-[(Dimethylamino)methyl]-4-fluoroaniline収率 72.8%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

反応条件

温度
55 °C

実験手順

A mix of satd. NH4Cl (5.19 mL) in EtOH (8 mL) was treated with 1-(2-fluoro-5-nitrophenyl)-N,N-dimethylmethanamine (494 mg, 2.49 mmol), followed by iron powder (1.39 g, 24.93 mmol) and heated at 55° C. overnight. The mixture was cooled to RT, the solids removed via filtration through diatomaceous earth and washed with 10% MeOH/DCM. The filtrate was concentrated to dryness, the residue treated with DCM, sonicated and the resulting solid collected via filtration, washed with THF and dried to afford 3-((dimethylamino)methyl)-4-fluoroaniline (305 mg, 72% yield). MS (ESI) m/z: 169.1 [M+H]+.

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

後処理

  1. additionA mix of satd
  2. temperatureThe mixture was cooled to RT
  3. customthe solids removed via filtration through diatomaceous earth
  4. washwashed with 10% MeOH/DCM
  5. concentrationThe filtrate was concentrated to dryness
  6. additionthe residue treated with DCM
  7. customsonicated
  8. filtrationthe resulting solid collected via filtration
  9. washwashed with THF
  10. customdried

出典と根拠

ORDレコード
ord-cdca075e005d4d23a9902568656447dd
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08461179B1

反応ノート

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