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5-Fluoro-2-(hydroxymethyl)benzoic acid → 5-Fluoro-2-formylbenzoic acid

HRID 2361287
ノート
印刷プレビュー

反応式

HRID 2361287 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

HCID 451570385-Fluoro-2-formylbenzoic acid収率 41.3%

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-73088f2ae7fb4ad3b9414e44c0a9ef94
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685969B2

反応ノート

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