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Diisobutylaluminumhydride → 2-(2-Bromo-4-fluorophenoxy)propionaldehyde

HRID 1824921
ノート
印刷プレビュー

反応式

HRID 1824921 の反応式
[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[C:6](OCC)=[O:7].[H-].C([Al+]CC(C)C)C(C)C>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[CH:6]=[O:7]
参加物反応条件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 21225700DiisobutylaluminumhydrideHCID 22144730Ethyl 2-(2'-bromo-4'-fluorophenoxy)propionate

生成物 1

HCID 221447442-(2-Bromo-4-fluorophenoxy)propionaldehyde収率 102.6%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
-78 °C

実験手順

A solution of 19.4 gm (66.7 mMol) ethyl 2-(2-bromo-4-fluorophenoxy)propionate in 400 mL toluene was cooled to −78° C. at which point 100 mL (100 mMol) diisobutylaluminum hydride (1 M in toluene) were added dropwise over 35 minutes. The reaction mixture was stirred at −78° C. for an additional 20 minutes after the addition was complete and then the reaction was quenched by the addition of methanol. The reaction mixture was warmed to room temperature and then treated with saturated aqueous sodium potassium carbonate. The mixture was stirred for 30 minutes and was then extracted well with ethyl acetate. The organic phases were combined, dried over sodium sulfate, and concentrated under reduced pressure to provide 16.9 gm of crude desired compound.

後処理

  1. additionwere added dropwise over 35 minutes
  2. additionafter the addition
  3. customthe reaction was quenched by the addition of methanol
  4. temperatureThe reaction mixture was warmed to room temperature
  5. additiontreated with saturated aqueous sodium potassium carbonate
  6. stirringThe mixture was stirred for 30 minutes
  7. extractionwas then extracted well with ethyl acetate
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-40821cd678f541069ddefc36a62680fe
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07045545B1

反応ノート

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