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Dimethylformamide → 2-Formyl-3-methyl-5-(4-methylphenyl)furan

HRID 22245
ノート
印刷プレビュー

反応式

HRID 22245 の反応式
P(Cl)(Cl)(Cl)=O.CN(C)[CH:8]=[O:9].[CH3:11][C:12]1[CH:16]=[C:15]([C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)[O:14][CH:13]=1.[OH-].[Na+]>ClC(Cl)C>[CH:8]([C:13]1[O:14][C:15]([C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)=[CH:16][C:12]=1[CH3:11])=[O:9]
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

6

反応物 4

HCID 6228DimethylformamideHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 13926387HCID 13926387、化合物

生成物 1

HCID 194301992-Formyl-3-methyl-5-(4-methylphenyl)furan

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane溶媒

反応条件

温度
0 °C

実験手順

Phosphorus oxychloride (12 ml) was added slowly to dimethylformamide (9.85 ml) with stirring at 0° C., and the mixture stirred at 0° C. for 30 minutes. A solution of 3-methyl-5-(4-methylphenyl)furan (22 g) in 50 ml of dichloroethane was added dropwise over a period of 15 minutes, maintaining the temperature at 0° C. The mixture was then stirred at room temperature for 11/2 hours. Ice water was then added, and the pH of the aqueous layer adjusted to about 8 with dilute sodium hydroxide. The organic layer was separated, the aqueous layer extracted with dichloromethane, the organic portions combined and solvent removed under reduced pressure. The solvent was removed from the filtrate under reduced pressure, and the residue flash chromatographed on silica gel, eluting with 10% ethyl acetate in heptane, to yield 19.2 g of 2-formyl-3-methyl-5-(4-methylphenyl)furan.

後処理

  1. stirringthe mixture stirred at 0° C. for 30 minutes
  2. temperaturemaintaining the temperature at 0° C
  3. stirringThe mixture was then stirred at room temperature for 11/2 hours
  4. customThe organic layer was separated
  5. extractionthe aqueous layer extracted with dichloromethane
  6. customsolvent removed under reduced pressure
  7. customThe solvent was removed from the filtrate under reduced pressure
  8. customthe residue flash chromatographed on silica gel
  9. washeluting with 10% ethyl acetate in heptane

出典と根拠

ORDレコード
ord-1d5091b33d1b49e295010bdab9394b2a
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05428037

反応ノート

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