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1-(6-Methoxy-benzofuran-3-yl)-ethane-1,2-diol → 6-Methoxybenzofuran-3-carbaldehyde

HRID 273336
ノート
印刷プレビュー

反応式

HRID 273336 の反応式
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[C:7]([CH:10]([OH:13])CO)=[CH:8][O:9][C:5]=2[CH:4]=1>C1COCC1.O>[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[C:7]([CH:10]=[O:13])=[CH:8][O:9][C:5]=2[CH:4]=1
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 691973081-(6-Methoxy-benzofuran-3-yl)-ethane-1,2-diol

生成物 1

HCID 824109866-Methoxybenzofuran-3-carbaldehyde収率 73%

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 8028Tetrahydrofuran溶媒

実験手順

NaIO4 (0.204 g, 1.12 mmol) was added to 1-(6-methoxy-benzofuran-3-yl)-ethane-1,2-diol (0.180 g, 1.196 mmol) in THF (50 mL) and water (1 mL) with stirring. The mixture was stirred overnight at room temperature under N2. Water (10 mL) was added, and the mixture was concentrated to half its volume and extracted with EtOAc. The organic layer was washed with brine and water, dried over anhyd. MgSO4, and evaporated to give a residue, which was purified on a silica gel column eluting with EtOAc/hexane (1:10) to give 6-methoxybenzofuran-3-carbaldehyde (0.110 g, 73%).

後処理

  1. stirringThe mixture was stirred overnight at room temperature under N2
  2. concentrationthe mixture was concentrated to half its volume
  3. extractionextracted with EtOAc
  4. washThe organic layer was washed with brine and water
  5. customdried over anhyd
  6. customMgSO4, and evaporated
  7. customto give a residue, which
  8. customwas purified on a silica gel column
  9. washeluting with EtOAc/hexane (1:10)

出典と根拠

ORDレコード
ord-48aeedf470cd4b08826f5be8112c6084
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07456289B2

反応ノート

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