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N-bromobutanimide → 3-bromo-5-fluoro-2-methylbenzoic acid

HRID 1187075
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인쇄 미리보기

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HRID 1187075 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].[Br:12]N1C(=O)CCC1=O>S(=O)(=O)(O)O>[Br:12][C:4]1[C:5]([CH3:11])=[C:6]([CH:10]=[C:2]([F:1])[CH:3]=1)[C:7]([OH:9])=[O:8]
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 1821145-Fluoro-2-methylbenzoic acid

생성물 1

HCID 666439353-bromo-5-fluoro-2-methylbenzoic acid

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

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온도
0 °C

실험 절차

To a cooled (0° C.) solution of 5-fluoro-2-methyl-benzoic acid (20 g, 130 mmol) in conc. sulfuric acid (200 mL) was added N-bromosuccinimide (24.3 g, 136 mmol) portionwise. The resulting mixture was stirred at 0° C. for 3 hrs, then warmed to room temperature and stirred for 16 hrs. Then the mixture was poured slowly into ice water (2 L), and extracted with EtOAc. The combined organic layers were washed with water and brine, dried and concentrated to provide 3-bromo-5-fluoro-2-methyl-benzoic acid, which was used directly in the next step.

후처리

  1. temperaturewarmed to room temperature
  2. stirringstirred for 16 hrs
  3. extractionextracted with EtOAc
  4. washThe combined organic layers were washed with water and brine
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a6c6c9106d84460a807180d1309caa0a
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673920B2

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