Hydrochloric Acid → HCID 58575185, 화합물

HRID 1807844노트

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HRID 1807844 반응식
C([NH:5][C:6]1[C:15]([N+:16]([O-:18])=[O:17])=[CH:14][C:9]([C:10]([O:12][CH3:13])=[O:11])=[C:8]([CH2:19][O:20][CH3:21])[CH:7]=1)(C)(C)C.Cl>CO>[NH2:5][C:6]1[C:15]([N+:16]([O-:18])=[O:17])=[CH:14][C:9]([C:10]([O:12][CH3:13])=[O:11])=[C:8]([CH2:19][O:20][CH3:21])[CH:7]=1

참가 물질

4

실험 절차

To a mixed liquid of 6.80 g of methyl 4-(tert-butylamino)-2-(methoxymethyl)-5-nitrobenzoate and 68.0 mL of methanol was added 37.0 mL of 6 M hydrochloric acid, followed by stirring overnight under the heating and refluxing condition. The solvent was evaporated under reduced pressure, and then 111 mL of methanol and 1.00 mL of concentrated sulfuric acid were added thereto, followed by stirring overnight under the heating and refluxing condition. Ethyl acetate and a saturated aqueous sodium hydrogen carbonate solution were added thereto, followed by extraction with ethyl acetate, the organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to obtain 4.73 g of methyl 4-amino-2-(methoxymethyl)-5-nitrobenzoate as a yellow solid.

후처리

  1. temperaturerefluxing condition
  2. customThe solvent was evaporated under reduced pressure
  3. addition111 mL of methanol and 1.00 mL of concentrated sulfuric acid were added
  4. stirringby stirring overnight under the heating and
  5. temperaturerefluxing condition
  6. additionEthyl acetate and a saturated aqueous sodium hydrogen carbonate solution were added
  7. extractionfollowed by extraction with ethyl acetate
  8. washthe organic layer was washed with saturated brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9f8a5c1fcd6646fe94a4750d7e8279d5
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08357688B2

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