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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Fluoro-2-(hydroxymethyl)benzoic acid → 5-Fluoro-2-formylbenzoic acid

HRID 2361287
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HRID 2361287 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:11][OH:12])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8]>O1CCCC1.[O-2].[Mn+4].[O-2]>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:11]=[O:12])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8]
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참가 물질

4

반응물 1

HCID 468313515-Fluoro-2-(hydroxymethyl)benzoic acid

생성물 1

HCID 451570385-Fluoro-2-formylbenzoic acid수율 41.3%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 5-fluoro-2-(hydroxymethyl)benzoic acid (0.518 g, 3.04 mmol) and manganese(IV) oxide (3.71 g, 42.6 mmol) in tetrahydrofuran (25 mL) was stirred at room temperature for 16 hr. The insoluble material was removed by filtration through CELITE®. The filtrate was concentrated under vacuum to dryness. The residue was dissolved in CH2Cl2 (100 mL) and dried over anhydrous MgSO4. Removal of solvent under vacuum provided the desired product (0.211 g, 1.255 mmol, 41.2% yield) as a white solid.

후처리

  1. customThe insoluble material was removed by filtration through CELITE®
  2. concentrationThe filtrate was concentrated under vacuum to dryness
  3. dissolutionThe residue was dissolved in CH2Cl2 (100 mL)
  4. dry with materialdried over anhydrous MgSO4
  5. customRemoval of solvent under vacuum

출처 및 근거

ORD 기록
ord-73088f2ae7fb4ad3b9414e44c0a9ef94
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08685969B2

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