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Chlorosuccinimide → 6-bromo-2-methyl-2,3-dihydro-1H-isoindol-1-one

HRID 216973
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HRID 216973 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:12])=[C:6]([CH:11]=1)[C:7](OC)=[O:8].Cl[N:14]1C(=O)CC[C:15]1=O>C(OCC)(=O)C>[Br:1][C:2]1[CH:11]=[C:6]2[C:5]([CH2:12][N:14]([CH3:15])[C:7]2=[O:8])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 316201Methyl 5-bromo-2-methylbenzoate

생성물 1

HCID 469420086-bromo-2-methyl-2,3-dihydro-1H-isoindol-1-one수율 10.1%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Methyl 5-bromo-2-methylbenzoate (3 g) in ethyl acetate (100 mL) was treated with N-chlorosuccinimide (1.749 g). The mixture was stirred and heated under reflux whilst being irradiated with a halogen lamp for 5 h. The reaction mixture was cooled and washed with 10% aqueous sodium metabisufite (100 mL) and water. The organic phase was dried over magnesium sulfate and concentrated to an oil. The crude product was treated with 8M methylamine in ethanol (20 mL) and the resulting mixture heated under reflux for 30 min. After cooling, the solution was concentrated to an oil, and the mixture purified on silica gel eluting with ethyl acetate to afford the sub-titled compound (0.300 g).

후처리

  1. temperatureheated
  2. temperatureunder reflux
  3. customwhilst being irradiated with a halogen lamp for 5 h
  4. temperatureThe reaction mixture was cooled
  5. washwashed with 10% aqueous sodium metabisufite (100 mL) and water
  6. dry with materialThe organic phase was dried over magnesium sulfate
  7. concentrationconcentrated to an oil
  8. additionThe crude product was treated with 8M methylamine in ethanol (20 mL)
  9. temperaturethe resulting mixture heated
  10. temperatureunder reflux for 30 min
  11. temperatureAfter cooling
  12. concentrationthe solution was concentrated to an oil
  13. customthe mixture purified on silica gel eluting with ethyl acetate

출처 및 근거

ORD 기록
ord-f044ff2bf4894776a71d7afacd6bb78c
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193239B2

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