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Water → 3-Bromo-6-hydroxy-2-methylbenzaldehyde

HRID 2036044
ノート
印刷プレビュー

反応式

HRID 2036044 の反応式
B(Br)(Br)Br.[Br:5][C:6]1[C:7]([CH3:16])=[C:8]([C:11]([O:14]C)=[CH:12][CH:13]=1)[CH:9]=[O:10].O.C(OCC)(=O)C.CCCCCC>ClCCl>[Br:5][C:6]1[C:7]([CH3:16])=[C:8]([C:11]([OH:14])=[CH:12][CH:13]=1)[CH:9]=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 25134Boron tribromideHCID 112416683-Bromo-6-methoxy-2-methylbenzaldehydeHCID 21226206Ethyl acetate hexane

生成物 1

HCID 156998303-Bromo-6-hydroxy-2-methylbenzaldehyde収率 73.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of boron tribromide (12.62 ml, 0.087 mol) in dichloromethane (50 ml) was added to a stirred solution of 3-Bromo-6-methoxy-2-methyl-benzaldehyde (20.0 g, 0.087 mol) in dichloromethane (350 ml) under nitrogen at 0° C. The reaction mixture was stirred for 1.5 hours. Water (400 ml) was added cautiously and the mixture was stirred for 15 min. The organic layer was washed with sodium bicarbonate solution (200 ml), water (200 ml) and brine (200 ml). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to give the crude product as orange brown solid. Column chromatography using 3/97 ethyl acetate/hexane yielded 3-Bromo-6-hydroxy-2-methyl-benzaldehyde (13.82 g, 73.6%).

後処理

  1. stirringthe mixture was stirred for 15 min
  2. washThe organic layer was washed with sodium bicarbonate solution (200 ml), water (200 ml) and brine (200 ml)
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto give the crude product as orange brown solid

出典と根拠

ORDレコード
ord-7483d5851a8f4b53802bad11263461c0
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08575161B2

反応ノート

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