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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 3-Nitro-5-vinylbenzoic acid methyl ester

HRID 1418276
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HRID 1418276 반응식
[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([CH:10]=[CH:11][Si](C)(C)C)[CH:7]=[C:6]([N+:16]([O-:18])=[O:17])[CH:5]=1.Cl>C(#N)C>[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([CH:10]=[CH2:11])[CH:7]=[C:6]([N+:16]([O-:18])=[O:17])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 543670333-Nitro-5-(2-trimethylsilylvinyl)benzoic acid methyl ester

생성물 1

HCID 540267313-Nitro-5-vinylbenzoic acid methyl ester

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3-Nitro-5-(2-trimethylsilylvinyl)benzoic acid methyl ester (2.44 g, 8.71 mmol) was dissolved in acetonitrile (150 ml), the solution was heated to reflux temperature and HCl gas was bubbled through the solution until the starting material had disappeared according to HPLC analysis. The solution was allowed to cool and the solvent was removed by evaporation. The residue was >95% pure according to HPLC and was used without further purification. Yield: 2.02 g (89%).

후처리

  1. temperaturethe solution was heated
  2. customwas bubbled through the solution until the starting material
  3. temperatureto cool
  4. customthe solvent was removed by evaporation
  5. customwas used without further purification

출처 및 근거

ORD 기록
ord-5a19b2cfdf1f4a75a6b2a1695005b892
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05882628

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