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Sulfuric Acid → 2-Bromo-5-methanesulfonyl-3-nitrothiophene

HRID 1192049
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HRID 1192049 반응식
[Br:1][C:2]1[S:3][C:4]([S:7]([CH3:10])(=[O:9])=[O:8])=[CH:5][CH:6]=1.S(=O)(=O)(O)O.[N+:16]([O-])([O-:18])=[O:17].[Na+]>>[Br:1][C:2]1[S:3][C:4]([S:7]([CH3:10])(=[O:9])=[O:8])=[CH:5][C:6]=1[N+:16]([O-:18])=[O:17]
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참가 물질

4

반응물 3

HCID 1118Sulfuric AcidHCID 24268Sodium NitrateHCID 173902812-Bromo-5-methanesulfonylthiophene

생성물 1

HCID 602073102-Bromo-5-methanesulfonyl-3-nitrothiophene수율 47%

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온도
0 °C

실험 절차

2-bromo-5-methylsulfonyl-thiophene (0.3 g, 1.24 mmol) was added to the concentrated sulfuric acid at 0° C. cooling in an ice bath. The resulted mixture was stirred at 0° C. for 5 minutes. Then sodium nitrate was introduced and the mixture was stirred at 0° C. for 1 hour. After this time, the reaction mixture was poured onto to the ice-water (10 mL) and was extracted with ethyl acetate. The organic phase was dried (Na2SO4) and concentrated under vacuum. The residue was purified by silica gel chromatography using a mixture of 95:5 hexane and ethyl acetate as eluent to afford the title product as a solid (0.17 g, 47% yield). 1H NMR (400 MHz, d6-DMSO) δ: 8.37 (1H, s), 2.50 (3H, m).

후처리

  1. temperaturecooling in an ice bath
  2. stirringthe mixture was stirred at 0° C. for 1 hour
  3. extractionwas extracted with ethyl acetate
  4. dry with materialThe organic phase was dried (Na2SO4)
  5. concentrationconcentrated under vacuum
  6. customThe residue was purified by silica gel chromatography
  7. additiona mixture of 95:5 hexane and ethyl acetate as eluent

출처 및 근거

ORD 기록
ord-33c4c7d703f04d47baa4856a3356cc41
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680139B2

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