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Sodium Carbonate → 2-(Thiophen-2-yl)benzaldehyde

HRID 1836678
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HRID 1836678 반응식
Br[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].C(=O)([O-])[O-].[Na+].[Na+].[S:16]1[CH:20]=[CH:19][CH:18]=[C:17]1B(O)O>COCCOC>[S:16]1[CH:20]=[CH:19][CH:18]=[C:17]1[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 811292-BromobenzaldehydeHCID 27339602-Thiopheneboronic acid

생성물 1

HCID 27955582-(Thiophen-2-yl)benzaldehyde

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

To a mixture of 2-bromobenzaldehyde (1.17 mL, 10.0 mmol) and 2.0 M aqueous sodium carbonate (75 mL) in DME (225 mL) were added thiophene-2-boronic acid (1.53 g, 12.0 mmol) and tetrakis(triphenylphosphine)palladium[0] (578 mg, 0.5 mmol). The mixture was heated to reflux under nitrogen for 16 hr. The resulting solution was cooled, and the crude product was extracted from aqueous solution with ethyl acetate. The organic layer was dried over MgSO4, and the solvents were removed under vacuum. The crude product was purified on flash column with 25% DCM in hexane to yield 2-(2-thienyl)benzaldehyde.

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후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux under nitrogen for 16 hr
  3. temperatureThe resulting solution was cooled
  4. extractionthe crude product was extracted from aqueous solution with ethyl acetate
  5. dry with materialThe organic layer was dried over MgSO4
  6. customthe solvents were removed under vacuum
  7. customThe crude product was purified on flash column with 25% DCM in hexane

출처 및 근거

ORD 기록
ord-f864db07518b4978bae3c45030eddb1c
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06777421B2

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