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

HRID 844495
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HRID 844495 반응식
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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

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

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온도
70 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-86da3c9ea37c4a0cabe7d6bbb071b881
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06380213B1

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