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Bromine → 4-Bromo-5-methylthiophene-2-carbaldehyde

HRID 453565
ノート
印刷プレビュー

反応式

HRID 453565 の反応式
[CH3:1][C:2]1[S:6][C:5]([CH:7]=[O:8])=[CH:4][CH:3]=1.[Br:9]Br.C(=O)([O-])O.[Na+]>C(O)(=O)C>[Br:9][C:3]1[CH:4]=[C:5]([CH:7]=[O:8])[S:6][C:2]=1[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24408BromineHCID 616635-Methyl-2-thiophenecarboxaldehydeHCID 516892Sodium Bicarbonate

生成物 1

HCID 155382124-Bromo-5-methylthiophene-2-carbaldehyde収率 50%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

To a solution of 5-methylthiophene-2-carbaldehyde (50.0 g) in acetic acid (400 mL) was added dropwise a solution of bromine (25 mL) in acetic acid (200 mL) at room temperature over 6 hr. After the dropwise addition, the reaction mixture was stirred overnight, neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was dissolved in toluene (50 mL), and the mixture was stirred at 110° C. for 2 hr and concentrated. The residue was subjected to silica gel column chromatography, eluted with ethyl acetate-hexane (1:5, volume ratio) and concentrated to give 4-bromo-5-methylthiophene-2-carbaldehyde (40.0 g, yield 50%) as yellow crystals. melting point 60° C.

後処理

  1. additionAfter the dropwise addition
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate layer was washed with saturated brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. dissolutionThe obtained residue was dissolved in toluene (50 mL)
  7. stirringthe mixture was stirred at 110° C. for 2 hr
  8. concentrationconcentrated
  9. washeluted with ethyl acetate-hexane (1:5, volume ratio)
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-a5c4e52c31994f848de269f47521ebcb
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08492405B2

反応ノート

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