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Phosphorus oxychloride → 2-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde

HRID 993447
ノート
印刷プレビュー

反応式

HRID 993447 の反応式
CN([CH:9]=[O:10])C1C=CC=CC=1.P(Cl)(Cl)(Cl)=O.[CH3:16][C:17]1[CH:18]=[C:19]([O:23][CH2:24][CH:25]=[CH2:26])[CH:20]=[CH:21][CH:22]=1>>[CH2:24]([O:23][C:19]1[CH:20]=[CH:21][C:22]([CH:9]=[O:10])=[C:17]([CH3:16])[CH:18]=1)[CH:25]=[CH2:26]
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 3

HCID 24813Phosphorus oxychlorideHCID 66737N-MethylformanilideHCID 2412733-Methyl-allyloxybenzene

生成物 1

HCID 222420922-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde収率 81%

反応条件

温度
70 °C

実験手順

N-methyl formanilide 19.4 ml (158 mmole), was chilled to 13° C., where it began to solidify. Phosphorus oxychloride, 13.7 ml (147 mmole), was added with stirring, under nitrogen. After 25 minutes, the temperature was 45° C. and the reaction had again begun to solidify. The compound of Step A, 14 g (95 mmole), was added and the mixture was stirred and heated in a 70° C. oil bath. The reaction exothermed to 95° C. Stirring was continued under nitrogen for 30 minutes. The bath was removed and when the temperature reached 350, the mixture was dissolved in chloroform. Ice was added and the layers were separated and washed once with water, twice with saturated sodium bicarbonate, once again with water and once with brine. The organic layer was chromatographed on 450 ml silica, eluting with chloroform to give 13.54 g (81%) of subtitled product which was used without further purification.

後処理

  1. customwas 45° C.
  2. stirringthe mixture was stirred
  3. customexothermed to 95° C
  4. stirringStirring
  5. waitwas continued under nitrogen for 30 minutes
  6. customThe bath was removed
  7. dissolutionthe mixture was dissolved in chloroform
  8. additionIce was added
  9. customthe layers were separated
  10. washwashed once with water, twice with saturated sodium bicarbonate, once again with water and once with brine
  11. customThe organic layer was chromatographed on 450 ml silica
  12. washeluting with chloroform

出典と根拠

ORDレコード
ord-040994d251d94ba6baa5b3c2f02021c6
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06472387B1

反応ノート

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