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Methyl 4-iodobenzoate → HCID 10236364, 화합물

HRID 1836045
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HRID 1836045 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9](B(O)O)=[CH:8][C:7]=2[CH:14]=1.I[C:16]1[CH:25]=[CH:24][C:19]([C:20]([O:22][CH3:23])=[O:21])=[CH:18][CH:17]=1>C1(C)C=CC=CC=1.CCO>[CH3:23][O:22][C:20](=[O:21])[C:19]1[CH:24]=[CH:25][C:16]([C:9]2[O:10][C:6]3[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:14][C:7]=3[CH:8]=2)=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 69273Methyl 4-iodobenzoateHCID 22221596(5-Methoxy-1-benzofuran-2-yl)boronic acid

생성물 1

HCID 10236364HCID 10236364, 화합물수율 32%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 1140Toluene용매

실험 절차

A solution of 5-Methoxy-benzofuran-2-boronic acid (1.9 g, 10 mmol), Methyl 4-iodobenzoate (2.61 g, 10 mmol), Pd(Ph3)4 (0.25 g), and 2M NaCO3 (10 ml) in toluene (40 ml) and EtOH (10 ml) was heated to reflux. After 2 hr, the reaction was cooled and the organic layer was seperated dried, and concentrated to give a solid. The solid was triturated with MeOH, filtered to give 127 (0.90 g, 32%) which was used without further purification or characterization for the next step.

후처리

  1. temperaturethe reaction was cooled
  2. customthe organic layer was seperated
  3. customdried
  4. concentrationconcentrated
  5. customto give a solid
  6. customThe solid was triturated with MeOH
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-439c105a8a844ce5a531f1d4e9c782c0
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06774248B2

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