Hydrogen Bromide → methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate

HRID 41527

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HRID 41527 반응식
[Br:1][C:2]1[CH:8]=[C:7]([Cl:9])[C:5](N)=[C:4]([Cl:10])[CH:3]=1.Br.N([O-])=O.[Na+].[C:16]([O:20][CH3:21])(=[O:19])[CH:17]=[CH2:18]>CC(C)=O.O>[Br:1][C:2]1[CH:8]=[C:7]([Cl:9])[C:5](/[CH:18]=[CH:17]/[C:16]([O:20][CH3:21])=[O:19])=[C:4]([Cl:10])[CH:3]=1

참가 물질

7

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온도
0 °C

실험 절차

4-Bromo-2,6-dichloroaniline (5, 80 g) was dissolved in acetone (640 mL), and a 48% hydrogen bromide aqueous solution (120 mL) was added, followed by stirring at 0° C. A sodium nitrite (32 g) aqueous solution (160 mL) was added dropwise thereto, the mixture was stirred for 30 minutes, and methyl acrylate (200 mL), and water (200 mL) were added, followed by stirring for 1 hour. At room temperature, cuprous oxide (2 g) was added, followed by stirring for 2 hours. The reaction solution was extracted with ethyl acetate, and purified by column chromatography to obtain methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate (48.5 g). Methyl (E)-3-(4-bromo-2,6-dichlorophenyl)acrylate (48.5 g) was dissolved in dichloromethane, an ozone gas was introduced at −70° C., and ozone oxidization was performed. To the reaction solution was added dimethyl sulfide (40 mL), and this was extracted with ethyl acetate to obtain 4-bromo-2,6-dichlorobenzaldehyde (6, 37.2 g).

후처리

  1. stirringthe mixture was stirred for 30 minutes
  2. stirringby stirring for 1 hour
  3. stirringby stirring for 2 hours
  4. extractionThe reaction solution was extracted with ethyl acetate
  5. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-65c93b62f49045c58e2bff1318798513
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08530668B2

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