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Ammonia → 2-[4-(2-Aminoethyl)phenyl]ethylamine

HRID 48363
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HRID 48363 반응식
[C:1]1([CH2:10][C:11]#[N:12])[CH:6]=[CH:5][C:4]([CH2:7][C:8]#[N:9])=[CH:3][CH:2]=1.N.[H][H]>[Ni].CO>[NH2:9][CH2:8][CH2:7][C:4]1[CH:5]=[CH:6][C:1]([CH2:10][CH2:11][NH2:12])=[CH:2][CH:3]=1
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참가 물질

6

반응물 3

HCID 222AmmoniaHCID 693271,4-BenzenediacetonitrileHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 27498872-[4-(2-Aminoethyl)phenyl]ethylamine수율 98%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

Scheme I, step B′: Into a 250 mL reduction vessel were placed 1,4-phenylenediacetonitrile (10 g, 64.02 mmol), liquid ammonia (25 mL), and W4-W6 range (medium range activity) Raney Nickel (1.25 g) in methanol (125 mL), and the mixture was heated at 100° C. under 300 psi (2068 kPa) of hydrogen gas for 10 hours. The reaction was cooled to room temperature and filtered through a Celite® cake and the filtrate was concentrated under reduced vacuum to give the intermediate title compound, 2-[4-(2-aminoethyl)phenyl]ethylamine, (10.3 g, 98%) as an oil. Electron spray M.S. 165 (M*+H).

후처리

  1. customScheme I, step B′: Into a 250 mL reduction vessel were placed
  2. filtrationfiltered through a Celite® cake
  3. concentrationthe filtrate was concentrated under reduced vacuum

출처 및 근거

ORD 기록
ord-80862a1fbb344d8d94617c30b01cc0a7
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06703425B2

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