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

HRID 1853920
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HRID 1853920 반응식
[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
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참가 물질

6

반응물 3

HCID 222AmmoniaHCID 4311764Sodium borohydrideHCID 219385811-(4-Bromo-2-fluorophenyl)ethan-1-one

생성물 1

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

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매HCID 887Methanol
용매

실험 절차

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]+.

후처리

  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

출처 및 근거

ORD 기록
ord-e98eb4c1e44b4e0a94bb08d3bfb9eb2f
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962648B2

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