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Toluene → 4-(4-Methoxy-3-methylphenyl)benzoic acid

HRID 1242801
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HRID 1242801 반응식
[CH3:1][C:2]1[CH:3]=[C:4](B(O)O)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].I[C:14]1[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C1(C)C=CC=CC=1>C(O)CCC.O>[CH3:1][C:2]1[CH:3]=[C:4]([C:14]2[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1140TolueneHCID 10796Cesium carbonateHCID 120854-Iodobenzoic acidHCID 2773487(4-Methoxy-3-methylphenyl)boronic acid

생성물 1

HCID 219394194-(4-Methoxy-3-methylphenyl)benzoic acid수율 30.3%

시약·촉매·용매 2

HCID 2631-Butanol용매
HCID 962Water용매

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온도
80 °C

실험 절차

3-Methyl-4-methoxyphenylboronic acid (542 mg) was combined with 4-iodobenzoic acid (810 mg), cesium carbonate (5.32 g), toluene (16 mL), water (8 mL) and n-butanol (4 mL). The mixture was degassed under vacuum with argon purging after which, tetrakis-triphenylphosphine palladium (38 mg) was added. The reaction was heated to 80° C. for 20 hours after which, it was cooled to room temperature and diluted with ethyl acetate (16 mL). The layers were separated and the organics were concentrated to dryness. The residue was purified on silica gel (50% to 100% ethyl acetate/hexane over 40 minutes) giving 3′-methyl-4′-methoxy-4-biphenylcarboxylic acid (240 mg). Yield=30%

후처리

  1. customThe mixture was degassed under vacuum with argon purging after which, tetrakis-triphenylphosphine palladium (38 mg)
  2. additionwas added
  3. temperaturewas cooled to room temperature
  4. additiondiluted with ethyl acetate (16 mL)
  5. customThe layers were separated
  6. concentrationthe organics were concentrated to dryness
  7. customThe residue was purified on silica gel (50% to 100% ethyl acetate/hexane over 40 minutes)

출처 및 근거

ORD 기록
ord-f9d29adc889840bbb96747d0034ffe83
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115741B2

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