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Sulfuric Acid → (S)-3-((4-Bromophenyl)amino)butanamide

HRID 2366845
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HRID 2366845 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C@@H:9]([CH3:13])[CH2:10][C:11]#[N:12])=[CH:4][CH:3]=1.[OH:14]S(O)(=O)=O>C1(C)C=CC=CC=1.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C@@H:9]([CH3:13])[CH2:10][C:11]([NH2:12])=[O:14])=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 1118Sulfuric AcidHCID 67173345(3S)-3-[(4-bromophenyl)amino]butanenitrile

생성물 1

HCID 67173762(S)-3-((4-Bromophenyl)amino)butanamide

시약·촉매·용매 2

HCID 962Water용매HCID 1140Toluene용매

반응 조건

온도
60 °C

실험 절차

(3S)-3-[(4-bromophenyl)amino]butanenitrile (for a preparation see Intermediate 32) (17.3 g, 72.4 mmol) was taken up in Toluene (500 ml) and H2SO4 (19.28 ml, 362 mmol) added. The biphasic mixture was stirred at 60° C. After two hours, only a small amount of SM remained by LCMS so the reaction was diluted with water (500 ml) and the phases separated. The aqueous phase was basified with 10N NaOH and extracted with EtOAc (2×750 ml). The combined organics were dried with Na2SO4, filtered and concentrated to yield the product as a cream solid (17.5 g). LCMS (Method B): Rt=0.77, MH+=257

후처리

  1. customthe phases separated
  2. extractionextracted with EtOAc (2×750 ml)
  3. dry with materialThe combined organics were dried with Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c55a6635b0ce492284de95485ad441c1
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08697725B2

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