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Ammonia → 1-(4-Bromo-2-fluorophenyl)ethan-1-amine

HRID 1853920
ノート
印刷プレビュー

反応式

HRID 1853920 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH3:9])=[C:4]([F:11])[CH:3]=1.[NH3:12].[BH4-].[Na+]>CO.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH2:12])[CH3:9])=[C:4]([F:11])[CH:3]=1
参加物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 222AmmoniaHCID 4311764Sodium borohydrideHCID 219385811-(4-Bromo-2-fluorophenyl)ethan-1-one

生成物 1

HCID 185435761-(4-Bromo-2-fluorophenyl)ethan-1-amine収率 63%

試薬・触媒・溶媒 2

HCID 11026Titanium isopropoxide触媒HCID 887Methanol溶媒

実験手順

To a solution of 1-(4-bromo-2-fluorophenyl)ethanone (2.0 g, 9.2 mmol) in methanol (50 mL) was added ammonia (7 N in methanol, 8.0 mL, 55 mmol) and titanium(IV) isopropoxide (5.4 mL, 18 mmol). The reaction mixture was stirred at room temperature for 18 h, cooled to 0° C. and sodium borohydride (520 mg, 14 mmol) was added. The reaction mixture was warmed to room temperature, stirred for 20 min, quenched with 2 M ammonium hydroxide and filtered. The reaction mixture was extracted with methylene chloride and the combined organic layers were dried over sodium sulfate, filtered, and concentrated to afford the desired product (1.2 g, 63%) as an oil: ESI MS m/z 219 [C8H9BrFN+H]+.

後処理

  1. temperaturecooled to 0° C.
  2. temperatureThe reaction mixture was warmed to room temperature
  3. stirringstirred for 20 min
  4. customquenched with 2 M ammonium hydroxide
  5. filtrationfiltered
  6. extractionThe reaction mixture was extracted with methylene chloride
  7. dry with materialthe combined organic layers were dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-e98eb4c1e44b4e0a94bb08d3bfb9eb2f
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08962648B2

反応ノート

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