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N-bromobutanimide → 2-Amino-5-bromo-4-fluoro-benzoic acid

HRID 2174327
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HRID 2174327 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Br:12]N1C(=O)CCC1=O>CN(C)C=O>[NH2:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([Br:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 27249674-Fluoroanthranilic acid

생성물 1

HCID 288272572-Amino-5-bromo-4-fluoro-benzoic acid수율 98.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

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온도
-10 °C

실험 절차

To a solution of 2-amino-4-fluorobenzoic acid (10 g, 64.5 mmol) in N,N-dimethylformamide (100 mL) at −10° C., was added dropwise a solution of N-bromosuccinimide (11.2 g, 62.9 mmol) in N,N-dimethylformamide (50 mL) over 1 hour. After the addition was complete, the mixture was stirred at −10° C. for 1 hour. The reaction was quenched with aqueous sodium bisulfate and partitioned between ethyl acetate and water. The organic layer was separated, and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with water and then with brine, and then dried over sodium sulfate. The sample was concentrated to give the crude product 27 (14.5 g, yield: 96.5%), which was used for the next step without further purification.

후처리

  1. additionAfter the addition
  2. customThe reaction was quenched with aqueous sodium bisulfate
  3. custompartitioned between ethyl acetate and water
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted twice with ethyl acetate
  6. washThe combined organic layers were washed with water
  7. dry with materialwith brine, and then dried over sodium sulfate
  8. concentrationThe sample was concentrated

출처 및 근거

ORD 기록
ord-3f7a91a2acb742e59a13e66b35a835aa
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09061060B2

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