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Phosphorus oxychloride → 4-Allyloxy-2,6-dimethyl-benzaldehyde

HRID 993450
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HRID 993450 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:24][CH2:25][CH:26]=[CH2:27])[CH:20]=[C:21]([CH3:23])[CH:22]=1>>[CH2:25]([O:24][C:19]1[CH:20]=[C:21]([CH3:23])[C:22]([CH:9]=[O:10])=[C:17]([CH3:16])[CH:18]=1)[CH:26]=[CH2:27]
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참가 물질

4

반응물 3

HCID 24813Phosphorus oxychlorideHCID 66737N-MethylformanilideHCID 257959Allyl 3,5-dimethylphenyl ether

생성물 1

HCID 185158104-Allyloxy-2,6-dimethyl-benzaldehyde수율 51%

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온도
70 °C

실험 절차

N-methyl formanilide, 20.5 ml (166 mmole), was chilled to 13°, where it began to solidify. Phosphorus oxychloride, 14.4 ml (155 mmole), was added with stirring, under nitrogen. After 25 minutes, the temperature was 450. 3,5-Dimethyl-allyloxy benzene, 16.2 g (100 mmole), prepared as describe above, was added with stirring and heated in a 70° C. oil bath. The reaction exothermed to 93° C. and was stirred under nitrogen for 30 minutes. The bath was removed and when the temperature reached 35°, the product was dissolved in chloroform. Ice was added, the layers were separated and washed once with water, twice with sodium bicarbonate, once with water and once with brine. The product was chromatographed down 500 ml of silica, eluting with chloroform to give 9.67 g (51%) of subtitled product which was used without further purification.

후처리

  1. additionwas added
  2. stirringwith stirring
  3. customexothermed to 93° C.
  4. stirringwas stirred under nitrogen for 30 minutes
  5. customThe bath was removed
  6. customreached 35°
  7. dissolutionthe product was dissolved in chloroform
  8. additionIce was added
  9. customthe layers were separated
  10. washwashed once with water, twice with sodium bicarbonate, once with water and once with brine
  11. customThe product was chromatographed down 500 ml of silica
  12. washeluting with chloroform

출처 및 근거

ORD 기록
ord-de43de8537b64e17915fb4a7fbff38f3
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06472387B1

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