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4-Nitro-1,2-bis(octyloxy)benzene → HCID 14980194, 화합물

HRID 1353136
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HRID 1353136 반응식
[CH2:1]([O:9][C:10]1[CH:11]=[C:12]([N+:25]([O-])=O)[CH:13]=[CH:14][C:15]=1[O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[H][H]>C(OCC)(=O)C.[Pd]>[CH2:1]([O:9][C:10]1[CH:11]=[C:12]([CH:13]=[CH:14][C:15]=1[O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[NH2:25])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 140913894-Nitro-1,2-bis(octyloxy)benzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 14980194HCID 14980194, 화합물수율 97%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

3,4-Dioctyloxynitrobenzene (25.25 g, 0.067 mol) was dissolved in ethyl acetate (250 mL) in a Parr bottle. 10% Pd on charcoal (3.5 g) was added and the mixture was hydrogenated (5–6 hr) at 50 psi until the hydrogen uptake ceased. The reaction mixture was filtered and evaporated. The aniline was obtained as a dark syrup. (22.5 g, 0.064 mol, 97% yield).

후처리

  1. custom(5–6 hr)
  2. filtrationThe reaction mixture was filtered
  3. customevaporated

출처 및 근거

ORD 기록
ord-69af30017f9d47fc8076681a882bbe86
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07220868B2

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