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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 3,5-Dimethyl-1-benzofuran-2-carbaldehyde

HRID 2091125
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HRID 2091125 반응식
CON(C)[C:4]([C:6]1[O:7][C:8]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][C:9]=2[C:10]=1[CH3:11])=[O:5].[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[CH3:11][C:10]1[C:9]2[CH:12]=[C:13]([CH3:16])[CH:14]=[CH:15][C:8]=2[O:7][C:6]=1[CH:4]=[O:5]
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참가 물질

5

반응물 3

HCID 962WaterHCID 21226445Aluminium lithium hydrideHCID 86662731N-methoxy-N,3,5-trimethyl-1-benzofuran-2-carboxamide

생성물 1

HCID 31596873,5-Dimethyl-1-benzofuran-2-carbaldehyde수율 74%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution (50 mL) of N-methoxy-N,3,5-trimethyl-1-benzofuran-2-carboxamide (3.78 g) synthesized above in tetrahydrofuran was added lithium aluminum hydride (307 mg) at −78° C., and the mixture was stirred for 2 hr. Water (350 μL) was added to quench the reaction, 1N aqueous sodium hydroxide solution (700 μL) was added, and the mixture was stirred at room temperature for 1 hr. The resulting insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was washed with hexane to give the title object compound (2.08 g, 74%) as a yellow solid.

후처리

  1. customto quench
  2. customthe reaction, 1N aqueous sodium hydroxide solution (700 μL)
  3. additionwas added
  4. stirringthe mixture was stirred at room temperature for 1 hr
  5. filtrationThe resulting insoluble material was filtered off
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. washThe residue was washed with hexane

출처 및 근거

ORD 기록
ord-b6383a2e2396445885fc0ac1aade4f05
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436043B2

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