Pyridine → HCID 21542801, 화합물

HRID 1606400

반응식

HRID 1606400 반응식
[Br:1][CH:2]1[CH:12]([Br:13])[CH2:11][CH2:10][CH:4]2[C:5]([NH:7][C:8](=[O:9])[CH:3]12)=[O:6].N1C=CC=CC=1.[Cl:20][C:21]1[C:26]([C:27](Cl)=[O:28])=[C:25]([Cl:30])[C:24]([Cl:31])=[C:23]([Cl:32])[C:22]=1[Cl:33]>C1C=CC=CC=1>[Cl:20][C:21]1[C:26]([C:27]([N:7]2[C:8](=[O:9])[CH:3]3[CH:2]([Br:1])[CH:12]([Br:13])[CH2:11][CH2:10][CH:4]3[C:5]2=[O:6])=[O:28])=[C:25]([Cl:30])[C:24]([Cl:31])=[C:23]([Cl:32])[C:22]=1[Cl:33]

참가 물질

5

반응물 3

HCID 1049PyridineHCID 1812012Pentachlorobenzoyl chlorideHCID 215427963,4-Dibromohexahydrophthalimide

생성물 1

HCID 21542801HCID 21542801, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

3,4-Dibromohexahydrophthalimide (0.10 mole), benzene (300 ml) and pyridine (0.11 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Pentachlorobenzoyl chloride (0.10 mole) is then added dropwise to the flask with stirring at room temperature. After the addition is completed the reaction mixture is heated at reflux with continued stirring for a period of about 1 hour. After this time the reaction mixture is filtered and the filtrate is washed with water. The washed filtrate is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-(pentachlorobenzoyl)-3,4-dibromohexahydrophthalimide.

후처리

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. additionAfter the addition
  4. temperatureis heated
  5. temperatureat reflux
  6. stirringwith continued stirring for a period of about 1 hour
  7. filtrationAfter this time the reaction mixture is filtered
  8. washthe filtrate is washed with water
  9. dry with materialThe washed filtrate is then dried over anhydrous magnesium sulfate
  10. filtrationfiltered

출처 및 근거

ORD 기록
ord-4147976ea91b4fe4bf352f1d59806c08
출처 데이터셋
uspto-grants-1976_04
특허 번호
US03953397

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