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Hydrochloric Acid → HCID 54158343, 화합물

HRID 255676
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HRID 255676 반응식
C([O:3][C:4]([CH:6]=[CH:7][C:8]1[N:9]([C:18]2[CH:23]=[CH:22][C:21]([OH:24])=[CH:20][C:19]=2[CH3:25])[CH:10]=[C:11]([C:15](=[O:17])[CH:16]=1)[C:12]([OH:14])=[O:13])=[O:5])C.Cl>C(OCC)C>[C:4]([CH:6]=[CH:7][C:8]1[N:9]([C:18]2[CH:23]=[CH:22][C:21]([OH:24])=[CH:20][C:19]=2[CH3:25])[CH:10]=[C:11]([C:15](=[O:17])[CH:16]=1)[C:12]([OH:14])=[O:13])([OH:5])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 70435233HCID 70435233, 화합물

생성물 1

HCID 54158343HCID 54158343, 화합물수율 96.8%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To 0.09 g of 6-(2-ethoxycarbonylethenyl)-1-(4-hydroxy-2-methylphenyl)-4-oxo-1,4-dihydronicotinic acid was added 3 ml of 6N hydrochloric acid, and they were reacted at 100° C. for 1.5 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and to the crystals thus formed were added 3 ml of diethyl ether, and the resulting mixture was filtered to obtain 0.08 g of 6-(2-carboxyethenyl)-1-(4-hydroxy-2-methylphenyl)-4-oxo-1,4-dihydronicotinic acid having a melting point of 280° C. or more.

후처리

  1. customwere reacted at 100° C. for 1.5 hours
  2. customAfter completion of the reaction
  3. customthe solvent was removed by distillation under reduced pressure
  4. customto the crystals thus formed
  5. filtrationthe resulting mixture was filtered

출처 및 근거

ORD 기록
ord-b6a60045473d45cb9fa453267c19ae2a
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04698352

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