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4,4'-((((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(5-(2-methoxyethoxy)-2-nitrobenzonitrile) → 4,4'-((((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(2-amino-5-(2-methoxyethoxy)benzonitrile)

HRID 1405960
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HRID 1405960 반응식
[O:1]([CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][C:30]1[C:37]([O:38][CH2:39][CH2:40][O:41][CH3:42])=[CH:36][C:33]([C:34]#[N:35])=[C:32]([N+:43]([O-])=O)[CH:31]=1)[CH2:2][CH2:3][O:4][CH2:5][CH2:6][O:7][C:8]1[C:15]([O:16][CH2:17][CH2:18][O:19][CH3:20])=[CH:14][C:11]([C:12]#[N:13])=[C:10]([N+:21]([O-])=O)[CH:9]=1>CC(O)=O.CC(O)C.[Fe]>[O:1]([CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][C:30]1[C:37]([O:38][CH2:39][CH2:40][O:41][CH3:42])=[CH:36][C:33]([C:34]#[N:35])=[C:32]([NH2:43])[CH:31]=1)[CH2:2][CH2:3][O:4][CH2:5][CH2:6][O:7][C:8]1[C:15]([O:16][CH2:17][CH2:18][O:19][CH3:20])=[CH:14][C:11]([C:12]#[N:13])=[C:10]([NH2:21])[CH:9]=1
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참가 물질

5

반응물 1

HCID 867011904,4'-((((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(5-(2-methoxyethoxy)-2-nitrobenzonitrile)

생성물 1

HCID 867011914,4'-((((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(2-amino-5-(2-methoxyethoxy)benzonitrile)수율 81%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 176Acetic Acid용매
HCID 3776
Isopropanol
용매

실험 절차

To a solution of 4,4′-((((oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(5-(2-methoxyethoxy)-2-nitrobenzonitrile) (0.3 g) in AcOH (10 mL) and i-PrOH (10 mL) was added iron powder (0.75 g). The resulting mixture was heated to reflux for 1 h. After reaction finished, the mixture was cooled to room temperature, filtered, the precipitate washed with EA (10 mL). The combined washings and filtrate were concentrated under reduced pressure and purification by silica chromatography to give 0.22 g of 4,4′-((((oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))-bis(oxy))bis(2-amino-5-(2-methoxyethoxy)benzonitrile). 1H-NMR (400 MHz, CDCl3): δ: 6.88 (s, 2H), 6.33 (s, 2H), 4.28 (br, 4H), 4.15-4.12 (m, 4H), 4.05-4.02 (m, 4H), 3.86-3.83 (m, 4H), 3.72-3.68 (m, 8H), 3.66-3.64 (m, 4H), 3.42 (s, 6H).

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureto reflux for 1 h
  3. customAfter reaction
  4. filtrationfiltered
  5. washthe precipitate washed with EA (10 mL)
  6. concentrationThe combined washings and filtrate were concentrated under reduced pressure and purification by silica chromatography

출처 및 근거

ORD 기록
ord-d1272a8fdcf14ea09df3af6e0c1da569
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916572B2

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