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N,N-diethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine → 4-(1-(Diethylamino)-2-methylpropan-2-yl)aniline

HRID 2423227
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HRID 2423227 반응식
[CH2:1]([N:3]([CH2:17][CH3:18])[CH2:4][C:5]([CH3:16])([C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][CH:8]=1)[CH3:6])[CH3:2]>[Pd].C(OCC)(=O)C>[CH2:17]([N:3]([CH2:1][CH3:2])[CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][CH:8]=1)([CH3:6])[CH3:16])[CH3:18]
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참가 물질

4

반응물 1

HCID 67242349N,N-diethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine

생성물 1

HCID 672414654-(1-(Diethylamino)-2-methylpropan-2-yl)aniline수율 93.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

In a 100 mL round bottomed flask was charged N,N-diethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine (1.45 g, 5.79 mmol), ethyl acetate (29 mL) and a nitrogen atmosphere was introduced to the flask. 10% Palladium on activated carbon was carefully introduced and the flask contents were purged (evacuate—backfill) twice with nitrogen and lastly with hydrogen dispensed from a balloon. The reaction was stirred for 16 h under the hydrogen atmosphere. The hydrogen was removed and the solution was filtered over Celite®, rinsed with methanol and the filtrate was concentrated in vacuo to give 4-(1-(diethylamino)-2-methylpropan-2-yl)aniline (1.19 g, 93.5%) as a light yellow oil. LC/MS (ESI+) 221 (M+H)+.

후처리

  1. additiona nitrogen atmosphere was introduced to the flask
  2. customthe flask contents were purged
  3. custom(evacuate—backfill) twice with nitrogen
  4. customThe hydrogen was removed
  5. filtrationthe solution was filtered over Celite®
  6. washrinsed with methanol
  7. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-c02448c117354a8a9f425b8525f5b8ae
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960569B2

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