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2-chloro-1-[(E)-2-nitroethenyl]-4-(trifluoromethyl)benzene → 2-(2-Chloro-4-(trifluoromethyl)phenyl)ethanamine

HRID 1021458
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HRID 1021458 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1/[CH:12]=[CH:13]/[N+:14]([O-])=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:10])([F:11])[F:9])[CH:5]=[CH:4][C:3]=1[CH2:12][CH2:13][NH2:14]
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참가 물질

4

반응물 2

HCID 57031342-chloro-1-[(E)-2-nitroethenyl]-4-(trifluoromethyl)benzeneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 670804752-(2-Chloro-4-(trifluoromethyl)phenyl)ethanamine수율 42.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

(E)-2-chloro-1-(2-nitrovinyl)-4-(trifluoromethyl)benzene (160 mg, 0.636 mmol) was diluted with THF (1 mL), placed under nitrogen and cooled to 0° C. LAH (2544 μL, 2.54 mmol) was added dropwise and the reaction was stirred for 5 hours warming to ambient temperature. The reaction was cooled to 0° C. and quenched with 100 μL of water, 100 μL of 15% NaOH and 300 μL water. After stirring for 1 hour, ethyl acetate and MgSO4 was added. The reaction mixture was filtered and concentrated to yield 2-(2-chloro-4-(trifluoromethyl)phenyl)ethanamine (60 mg, 0.268 mmol, 42.2% yield).

후처리

  1. temperaturewarming to ambient temperature
  2. temperatureThe reaction was cooled to 0° C.
  3. customquenched with 100 μL of water, 100 μL of 15% NaOH and 300 μL water
  4. stirringAfter stirring for 1 hour
  5. additionethyl acetate and MgSO4 was added
  6. filtrationThe reaction mixture was filtered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b5761b2f16a84882ba4ed15d61826c90
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716498B2

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