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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Bicarbonate → HCID 57652724, 화합물

HRID 1013265
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HRID 1013265 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:20][CH3:21])[CH:8]=[C:9]([N+:11]([O-])=O)[CH:10]=1)=[O:4].C([O-])(O)=O.[Na+]>CCOC(C)=O>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:20][CH3:21])[CH:8]=[C:9]([NH2:11])[CH:10]=1)=[O:4]
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참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 57652728HCID 57652728, 화합물

생성물 1

HCID 57652724HCID 57652724, 화합물수율 98.2%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

2′-Methoxy-5-nitro-biphenyl-3-carboxylic acid methyl ester (8.2 g, 28.5 mmol) and SnCl2 dihydrate (35 g) in EtOAc (300 mL) was heated to reflux and stirred for 18 hours, then cooled and stirred at room temperature for 48 hours. Saturated aqueous NaHCO3 was added until the aqueous portion of the mixture reached pH 10. The organic layer was separated, and the aqueous layer was washed with EtOAc. The combined organic layers were washed with water, dried over Na2SO4, filtered and concentrated under reduced pressure to give 7.2 g of 5-amino-2′-methoxy-biphenyl-3-carboxylic acid methyl ester, MS (M+H)=258.

후처리

  1. temperatureto reflux
  2. temperaturecooled
  3. stirringstirred at room temperature for 48 hours
  4. customThe organic layer was separated
  5. washthe aqueous layer was washed with EtOAc
  6. washThe combined organic layers were washed with water
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9815b4a2e78f4c69937cb6436ffa99ee
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981914B2

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