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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(4-Phenyl-1,3-thiazol-2-yl)methanol → 4-Phenyl-1,3-thiazole-2-carbaldehyde

HRID 868928
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HRID 868928 반응식
[C:1]1([C:7]2[N:8]=[C:9]([CH2:12][OH:13])[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C(Cl)Cl.O=[Mn]=O>[C:1]1([C:7]2[N:8]=[C:9]([CH:12]=[O:13])[S:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 1

HCID 698895(4-Phenyl-1,3-thiazol-2-yl)methanol

생성물 1

HCID 35388144-Phenyl-1,3-thiazole-2-carbaldehyde수율 40.5%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

To (4-phenylthiazol-2-yl)methanol (900 mg, 4.7 mmol) in DCM (10 mL) was added MnO2 (4 g, 47 mmol), and the mixture was stirred at room temperature for 3 hours. The reaction mixture was then filtered, washed with water, extracted with EtOAc and dried over anhydrous sodium sulfate. The solution was concentrated under vacuum to give a crude product, which was purified by column chromatography to afford the title compound as a yellow solid (360 mg).

후처리

  1. filtrationThe reaction mixture was then filtered
  2. washwashed with water
  3. extractionextracted with EtOAc
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationThe solution was concentrated under vacuum
  6. customto give a crude product, which
  7. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-4bc28a79bd7741e2969c7d22eec64782
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969349B2

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