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Bromine → 3'-Bromo-4'-methoxy-1,1'-biphenyl-4-carbaldehyde

HRID 493479
ノート
印刷プレビュー

反応式

HRID 493479 の反応式
[Br:1]Br.[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([CH:17]=[O:18])=[CH:13][CH:12]=2)=[CH:7][CH:6]=1>CC(O)=O>[Br:1][C:10]1[CH:9]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([CH:17]=[O:18])=[CH:13][CH:12]=2)[CH:7]=[CH:6][C:5]=1[O:4][CH3:3]
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 2

HCID 24408BromineHCID 13944874'-Methoxy-(1,1'-biphenyl)-4-carboxaldehyde

生成物 1

HCID 576816103'-Bromo-4'-methoxy-1,1'-biphenyl-4-carbaldehyde収率 96%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

Bromine (8.2 mL, 0.160 mol) in 40 mL of glacial HOAc was added under nitrogen dropwise over 30 minutes to a solution of 4′-methoxy-1,1′-biphenyl-4-carbaldehyde (31.0g, 0.146 mol), prepared in the previous step, in 500 mL of glacial HOAc at room temperature. After the addition the reaction was stirred at room temperature for 16 h. During the reaction a solid precipitated. The solid can be collected by filtration. If by TLC starting material remains in either the solid or filtrate the solid can be redissolved and additional bromine added until the reaction is complete. When the reaction is complete by TLC, water is added and the solid present is collected by filtration to give 3′-bromo-4′-methoxy-1,1′-biphenyl-4-carbaldehyde (40.8 g, 96%) as a white solid, MS (ESI) m/z 290. Elemental Analysis for C14H11BrO2. Calc'd: C, 57.76; H, 3.81; N, 0.00. Found: C, 57.30; H, 3.61; N, 0.00.

後処理

  1. additionAfter the addition the reaction
  2. customDuring the reaction a solid
  3. customprecipitated
  4. filtrationThe solid can be collected by filtration
  5. dissolutioncan be redissolved
  6. additionadditional bromine added until the reaction
  7. additionis added
  8. filtrationthe solid present is collected by filtration

出典と根拠

ORDレコード
ord-0a1978b31d8f45b89dcb1093dcb980fc
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07534894B2

反応ノート

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