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Benzene, 1-nitro-3-[2-nitro-1-(nitromethyl)ethyl]- → HCID 86702440, 화합물

HRID 2203269
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HRID 2203269 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH2:15][N+:16]([O-])=O)[CH2:11][N+:12]([O-])=O)[CH:5]=1)([O-])=O.[H][H]>CO.[Pt](=O)=O>[NH2:1][C:4]1[CH:5]=[C:6]([CH:10]([CH2:15][NH2:16])[CH2:11][NH2:12])[CH:7]=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11230571Benzene, 1-nitro-3-[2-nitro-1-(nitromethyl)ethyl]-HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86702440HCID 86702440, 화합물

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol용매

실험 절차

A mixture of 1-nitro-3-[2-nitro-1-(nitromethyl)ethyl]benzene (115 mg, 0.45 mmol) and 58 mg platinum (IV) oxide in 6 mL MeOH contained in a pressure tube was reacted under 65 PSI hydrogen. After 16 hours the mixture was filtered and rinsed with MeOH. The MeOH solution of product was stored under N2 in the freezer and used as is for the next reaction [upon evaporation of MeOH solvent 69.9 mg (94%) of the title compound was obtained as a light yellow oil]. 1H NMR (CD3OD) δ: 7.06-7.13 (m, 1H), 6.55-6.65 (m, 3H), 2.83-2.91 (m, 2H), 2.72-2.81 (m, 2H), 2.57-2.68 (m, 1H).

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후처리

  1. customcontained in a pressure tube
  2. filtrationAfter 16 hours the mixture was filtered
  3. washrinsed with MeOH
  4. customas is for the next reaction [
  5. customupon evaporation of MeOH solvent 69.9 mg (94%) of the title compound
  6. customwas obtained as a light yellow oil]

출처 및 근거

ORD 기록
ord-0a7ef9ce788a494b820565998c7a6626
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365575B2

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