Potassium Hydroxide → 2'-Methoxy-[1,1';3',1"]terphenyl-5'-carboxylic acid

HRID 1067318노트

반응식

HRID 1067318 반응식
C[O:2][C:3]([C:5]1[CH:6]=[C:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:8]([O:17][CH3:18])=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:10]=1)=[O:4].[OH-].[K+]>C1COCC1.CCOCC>[CH3:18][O:17][C:8]1[C:9]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[CH:6][C:7]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 536767312'-Methoxy-[1,1';3',1"]terphenyl-5'-carboxylic acid methyl ester

생성물 1

HCID 234456322'-Methoxy-[1,1';3',1"]terphenyl-5'-carboxylic acid수율 95%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
100 °C

실험 절차

At ambient temperature, to a stirred solution of 2′-methoxy-[1,1′;3′,1″]terphenyl-5′-carboxylic acid methyl ester (1.148 g, 3.606 mmol) in THF (36.06 mL) was added 1N KOH (36.06 mL) and the reaction was stirred for 16 h. The reaction was heated at 100° C. for an additional 24 h. The reaction was cooled to ambient temperature, diluted with ether (100 mL) and extracted with 0.1N NaOH. The aqueous extracts were washed with ether (3×), acidified with 6N HCl and extracted with EtOAc. The organic extracts were dried (MgSO4) and concentrated to give 1.043 g (95%) of the title compound. 1H NMR (DMSO-d6) δ3.15 (s, 3H), 7.40-7.52 (m, 6H), 7.58-7.60 (m, 4H), 7.88 (s, 2H), 13.04 (s, 1H).

후처리

  1. temperatureThe reaction was cooled to ambient temperature
  2. extractionextracted with 0.1N NaOH
  3. washThe aqueous extracts were washed with ether (3×)
  4. extractionextracted with EtOAc
  5. dry with materialThe organic extracts were dried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ea5e23d9c19e4fa1b583d6435ddfa4f2
출처 데이터셋
uspto-grants-2001_06
특허 번호
US06248764B1

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