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Trifluoroacetic acid → 2,6-Diethoxy-4'-(methoxycarbonyl)biphenyl-4-carboxylic acid

HRID 38483
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HRID 38483 반응식
C(O)(C(F)(F)F)=O.[CH2:8]([O:10][C:11]1[CH:16]=[C:15]([C:17]([O:19]C(C)(C)C)=[O:18])[CH:14]=[C:13]([O:24][CH2:25][CH3:26])[C:12]=1[C:27]1[CH:32]=[CH:31][C:30]([C:33]([O:35][CH3:36])=[O:34])=[CH:29][CH:28]=1)[CH3:9]>C(Cl)(Cl)Cl>[CH2:25]([O:24][C:13]1[CH:14]=[C:15]([C:17]([OH:19])=[O:18])[CH:16]=[C:11]([O:10][CH2:8][CH3:9])[C:12]=1[C:27]1[CH:28]=[CH:29][C:30]([C:33]([O:35][CH3:36])=[O:34])=[CH:31][CH:32]=1)[CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 670555564-tert-Butyl 4'-methyl 2,6-diethoxybiphenyl-4,4'-dicarboxylate

생성물 1

HCID 670555482,6-Diethoxy-4'-(methoxycarbonyl)biphenyl-4-carboxylic acid

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

TFA (4 ml) was added to a stirred solution of 4-tert-butyl 4′-methyl 2,6-diethoxybiphenyl-4,4′-dicarboxylate (850 mg, 2.12 mmol) in CHCl3 (2 ml) and the reaction mixture was stirred at room temperature overnight. After the solvents were removed under reduced pressure, CHCl3 and MeOH were added to the residue. The solvents were removed under reduced pressure again, and the residue was dried in vacuo to give the crude intended compound as a colorless solid. Thus obtained crude product was used in the next step without further purification.

후처리

  1. customAfter the solvents were removed under reduced pressure, CHCl3 and MeOH
  2. additionwere added to the residue
  3. customThe solvents were removed under reduced pressure again
  4. customthe residue was dried in vacuo
  5. customto give the crude
  6. customThus obtained crude product
  7. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-9a75025d13f545a9afdab4eee5c8436d
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524730B2

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