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Hydrochloric Acid → 5-ethyl-4-phenyl-1H-imidazole

HRID 1747268
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HRID 1747268 반응식
Cl.[S-][C:3]#[N:4].[Na+].Cl.[NH2:7][CH:8]([CH3:17])[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O.[CH2:18](O)C>>[CH2:17]([C:8]1[NH:7][CH:3]=[N:4][C:9]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:18]
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 2046302-Amino-1-phenylpropan-1-one;hydrochlorideHCID 516871Sodium thiocyanate

생성물 1

HCID 142976295-ethyl-4-phenyl-1H-imidazole수율 45%

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온도
70 °C

실험 절차

An aqueous solution (5 mL) of concentrated hydrochloric acid (0.6 mL) and sodium thiocyanate (1.62 g, 20.03 mmol) was added to a solution of 2-aminopropiophenone hydrochloride (2.00 g, 10.02 mmol) in ethanol (20 mL). The obtained mixture was stirred at 70° C. for 1 hour. The solvent was distilled away, and acetic acid (20 mL) was then added to the residue. The obtained mixture was stirred at 100° C. for 3 hours. Thereafter, water was added to the reaction solution, and the precipitated crude crystals were collected by filtration. Raney Ni was added to a solution of the obtained crude crystals in ethanol (40 mL), and the obtained mixture was then stirred at 70° C. for 2 hours. The reaction solution was filtered with celite, and the filtrate was then concentrated. The residue was washed with acetonitrile, so as to obtain the title compound (0.88 g, yield in two steps: 45%).

후처리

  1. distillationThe solvent was distilled away
  2. additionacetic acid (20 mL) was then added to the residue
  3. stirringThe obtained mixture was stirred at 100° C. for 3 hours
  4. additionThereafter, water was added to the reaction solution
  5. customthe precipitated crude crystals
  6. filtrationwere collected by filtration
  7. additionRaney Ni was added to a solution of the
  8. customobtained crude crystals in ethanol (40 mL)
  9. stirringthe obtained mixture was then stirred at 70° C. for 2 hours
  10. filtrationThe reaction solution was filtered with celite
  11. concentrationthe filtrate was then concentrated
  12. washThe residue was washed with acetonitrile

출처 및 근거

ORD 기록
ord-f4ebad2b8c5349d5a6fadf91e1314cf6
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150563B2

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