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Dimethylformamide → 2-Isopropyl-6-methylbenzaldehyde

HRID 427510
ノート
印刷プレビュー

反応式

HRID 427510 の反応式
Br[C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH:9]([CH3:11])[CH3:10].[Mg].CN(C)[CH:15]=[O:16]>C(OCC)C>[CH:9]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([CH3:8])[C:2]=1[CH:15]=[O:16])([CH3:11])[CH3:10]
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 6228DimethylformamideHCID 5462224MagnesiumHCID 145345702-Bromo-1-isopropyl-3-methylbenzene

生成物 1

HCID 124670472-Isopropyl-6-methylbenzaldehyde収率 33%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a solution of 1-bromo-2-isopropyl-6-methylbenzene (6.9 g, 32.4 mmol) in diethyl ether (50 ml) was added magnesium turnings (0.9 g, 37 mmol) and the mixture was refluxed in nitrogen atmosphere until the reaction was started and was then stirred overnight at room temperature. Dimethylformamide (4 ml) was added dropwise during 10 min. and the mixture was stirred for 30 min. Saturated ammmoniumchloride solution (30 ml) was added and the mixture was stirred for 1 h. The organic layer was separated, filtrated and evaporated under reduced pressure. Purification by column chromatography on silica gel using hexane:methylene chloride (3:2) as eluent gave 1.75 g (33%) of the title compound .

後処理

  1. temperaturethe mixture was refluxed in nitrogen atmosphere until the reaction
  2. stirringthe mixture was stirred for 30 min
  3. stirringthe mixture was stirred for 1 h
  4. customThe organic layer was separated
  5. filtrationfiltrated
  6. customevaporated under reduced pressure
  7. customPurification by column chromatography on silica gel

出典と根拠

ORDレコード
ord-bb5ea198fbde4afeb2dd934f21b8792d
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313137B1

反応ノート

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