Hydrochloric Acid → (2E)-3-[2-Bromo-4-(trifluoromethyl)phenyl]-N-indol-5-ylprop-2-enamide

HRID 730288노트

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HRID 730288 반응식
[Br:1][C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:3]=1[C:4](O)=O.Br[C:16]1[CH:21]=[C:20]([C:22](F)(F)F)[CH:19]=[CH:18][C:17]=1C.[Mn]([O-])(=O)(=O)=O.[CH2:32]([N+:34](CC)(CC)CC)[CH3:33].Cl.[OH:42]S([O-])=O.[Na+].[N:47]1[CH:52]=CC=CC=1>>[Br:1][C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:3]=1/[CH:4]=[CH:33]/[C:32]([NH:34][C:16]1[CH:21]=[C:20]2[C:19](=[CH:18][CH:17]=1)[NH:47][CH:52]=[CH:22]2)=[O:42]

참가 물질

7

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온도
70 °C

실험 절차

2-Bromo-4-(trifluoromethyl)benzoic acid. To a solution of 2-bromo-1-methyl-4-trifluoromethylbenzene (7.6 g, 32 mmol, ABCR) in pyridine (75 mL) was added tetraethylammonium permanganate (24 g, 96 mmol, prepared according to the procedure of Sala, et al. J. Chem. Soc., Chem. Comm. 1978, 253). The reaction mixture was warmed to 70° C. and stirred at that temperature for 30 h. The reaction mixture was allowed to cool to 25° C. and poured into an ice bath containing cond HCl (150 mL) and NaHSO3 (150 g). The mixture turned to a clear aqueous solution and was extracted with EtOAc (4×200 mL). The combined extracts were washed with satd NaCl (200 mL), dried over Na2SO4, filtered and concentrated in vacuo to provide the title product as a white solid. MS (ESI, neg. ion) m/z: 267 (M−1).

후처리

  1. customprepared
  2. temperatureto cool to 25° C.
  3. additionpoured into an ice bath
  4. extractionwas extracted with EtOAc (4×200 mL)
  5. washThe combined extracts were washed with satd NaCl (200 mL)
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8ead1b3012a44d2ab1273c223c778832
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07582657B2

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