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Acetic Acid → Methyl 4-(2,2-dimethoxyethyl)-3-nitrobenzoate

HRID 1067754
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HRID 1067754 반응식
[CH3:1][O-:2].[Na+].[N+:4]([C:7]1[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=1[C:17]#[C:18][Si](C)(C)C)[C:10]([O:12][CH3:13])=[O:11])([O-:6])=[O:5].[C:23]([OH:26])(=O)C>CO>[CH3:1][O:2][CH:18]([O:26][CH3:23])[CH2:17][C:16]1[CH:15]=[CH:14][C:9]([C:10]([O:12][CH3:13])=[O:11])=[CH:8][C:7]=1[N+:4]([O-:6])=[O:5]
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 10942334Sodium MethoxideHCID 13585838Methyl 3-nitro-4-trimethylsilylethynylbenzoate

생성물 1

HCID 10265064Methyl 4-(2,2-dimethoxyethyl)-3-nitrobenzoate수율 82.5%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

To a methanol solution of 2.92 g (54.1 mmol) of sodium methoxide was added 3.00 g (10.8 mmol) of methyl 3-nitro-4-trimethylsilylethynylbenzoate prepared above. The mixture was refluxed for 30 minutes. After cooling to 0° C., 5.52 g (54.1 mmol) of acetic acid was added to the reaction mixture and the solvent was then distilled off under reduced pressure. Ice water was poured onto the resulting residue followed by extraction three times with dichloromethane. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography to give 2.40 g (82.4%) of methyl 4-(2,2-dimethoxyethyl)-3-nitrobenzoate.

후처리

  1. customprepared above
  2. temperatureThe mixture was refluxed for 30 minutes
  3. distillationthe solvent was then distilled off under reduced pressure
  4. additionIce water was poured onto the resulting residue
  5. extractionfollowed by extraction three times with dichloromethane
  6. dry with materialAfter drying over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-64e9e2d6c02d4f0dab2ca97ac44aec24
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06248772B1

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