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3-Bromo-4-chlorobenzamide → 3-Bromo-4-chlorobenzylamine

HRID 657360
ノート
印刷プレビュー

反応式

HRID 657360 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[C:5]([NH2:7])=O>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][NH2:7])[CH:8]=[CH:9][C:10]=1[Cl:11]
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

3

反応物 1

HCID 532166633-Bromo-4-chlorobenzamide

生成物 1

HCID 578133923-Bromo-4-chlorobenzylamine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

To 3-bromo-4-chlorobenzamide (1.6 g, 6.8 mmol) in THF (10 mL) was added borane dimethyl sulfide complex (1.36 mL, 13.6 mmol) at room temperature. The mixture was then heated to 60° C. for 8 days. The solvent was pumped off and the reaction cautiously quenched with ethanol. When bubbling ceased, 1N HCl was added until the pH was ˜2. The mixture was stirred at 50° C. for 4 h. The mixture was partitioned between EtOAc and water. The aqueous phase was washed 3× with EtOAc. The aqueous phase was then adjusted to pH 10 with 2N NaOH and extracted 3× with EtOAc. The combined organics phases were washed with brine, dried over anhydrous Na2SO4, filtered, and evaporated to afford the title compound as a clear oil. LC-MS m/z 219.6 (M+H)+, 1.41 min (ret time).

後処理

  1. customthe reaction
  2. customcautiously quenched with ethanol
  3. customWhen bubbling
  4. addition1N HCl was added until the pH was ˜2
  5. customThe mixture was partitioned between EtOAc and water
  6. washThe aqueous phase was washed 3× with EtOAc
  7. extractionextracted 3× with EtOAc
  8. washThe combined organics phases were washed with brine
  9. dry with materialdried over anhydrous Na2SO4
  10. filtrationfiltered
  11. customevaporated

出典と根拠

ORDレコード
ord-2111612c195645ad9d92bbf8fd1a5fc4
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071588B2

反応ノート

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