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Sodium borohydride → 3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)propanenitrile

HRID 474602
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HRID 474602 반응식
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]=[CH:14][C:15]#[N:16])=[CH:9][CH:8]=1.[BH4-].[Na+]>C(O)C>[F:1][C:2]([F:20])([F:21])[C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[O:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:13][CH2:14][C:15]#[N:16])=[CH:11][CH:12]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 677761303-(4-(3-(Trifluoromethyl)phenoxy)phenyl)acrylonitrile

생성물 1

HCID 677751713-(4-(3-(Trifluoromethyl)phenoxy)phenyl)propanenitrile수율 80.3%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
70 °C

실험 절차

To a solution of 3-(4-(3-(trifluoromethyl)phenoxy)phenyl)acrylonitrile (5 g, 17.29 mmol) in Ethanol (80 mL) was added NaBH4 (4.5 g, 119 mmol). The reaction mixture was stirred at 70° C. overnight. After cooling to room temperature, the reaction mixture was quenched with water (50 mL), and ethanol was removed under reduced pressure. The residue was partitioned between EA (100 mL) and water (50 mL). The organic phase was washed with saturated NaHCO3 solution (80 mL), brine (50 mL), dried over sodium sulfate, concentrated, and purified via flash chromatography to afford the title compound (4.3 g, 13.89 mmol, 80% yield) as colorless oil. LCMS: rt=1.64 min, no MS signal

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe reaction mixture was quenched with water (50 mL), and ethanol
  3. customwas removed under reduced pressure
  4. customThe residue was partitioned between EA (100 mL) and water (50 mL)
  5. washThe organic phase was washed with saturated NaHCO3 solution (80 mL), brine (50 mL)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated
  8. custompurified via flash chromatography

출처 및 근거

ORD 기록
ord-11328ee3dd9d4d91ae9e09eba409cea1
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637536B2

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