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2-Bromo-4-fluorobenzaldehyde → 2-Bromo-4-methoxybenzaldehyde

HRID 857357
ノート
印刷プレビュー

反応式

HRID 857357 の反応式
[Br:1][C:2]1[CH:9]=[C:8](F)[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[CH3:11][O-:12].[Na+].CO>CO.C(Cl)Cl.O>[Br:1][C:2]1[CH:9]=[C:8]([O:12][CH3:11])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5]
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 2

HCID 27733192-Bromo-4-fluorobenzaldehydeHCID 23694274Sodium methanolate methanol

生成物 1

HCID 111276412-Bromo-4-methoxybenzaldehyde

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 21908982Water methylene chloride溶媒

実験手順

To a solution of 2-bromo-4-fluorobenzaldehyde (50 g, 246 mmol), in MeOH (500 mL) in a 15° C. water bath was added a 25% solution of NaOMe/MeOH (88 mL). The mixture was stirred at r.t. for 1 hour followed by 2 hours at reflux. The solid was filtered and the filtrate was concentrated to dryness to give a second crop of solid. Both crops were taken up in CH2Cl2/H2O. After washing with H2O, the organic phase was dried (MgSO4), filtered, and evaporated to give an off-white solid (52.2 g).

後処理

  1. waitfollowed by 2 hours
  2. temperatureat reflux
  3. filtrationThe solid was filtered
  4. concentrationthe filtrate was concentrated to dryness
  5. customto give a second crop of solid
  6. washAfter washing with H2O
  7. dry with materialthe organic phase was dried (MgSO4)
  8. filtrationfiltered
  9. customevaporated

出典と根拠

ORDレコード
ord-4eff59624f9a47a0aac51d081ec53409
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07144913B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート