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Ammonium Chloride → HCID 178488534, compound

HRID 1059139
Notes
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Reaction equation

HRID 1059139 reaction equation
Br[C:2]1[N:3]=[CH:4][NH:5][CH:6]=1.C([Li])(C)(C)C.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:16][C:15]=1[CH:26]=[O:27].[Cl-].[NH4+]>C1COCC1.CCCCC>[NH:5]1[CH:6]=[C:2]([CH:26]([C:15]2[CH:16]=[C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:18]=[CH:19][C:14]=2[O:13][CH3:12])[OH:27])[N:3]=[CH:4]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 25517Ammonium ChlorideHCID 31596652-Methoxy-5-phenylbenzaldehydeHCID 178418306HCID 178418306, compoundHCID 178418934HCID 178418934, compound

Product 1

HCID 178488534HCID 178488534, compoundYield 34.3%

Reagents, catalysts & solvents 2

HCID 8003
Pentane
Solvent
HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-78 °C

Procedure

4-Bromo-1H-imidazole (5.20 g) was dissolved in THF (50 ml) and the mixture was cooled to −78° C. A solution (1.7 M; 50 ml) of t-butyllithium in pentane was added. The mixture was stirred at 0° C. for 1.5 h and cooled to −78° C. again. A solution (30 ml) of 4-methoxy[1,1′-biphenyl]-3-carbaldehyde (2.54 g) in THF was added, and the mixture was heated from −78° C. to room temperature and further stirred at room temperature for 24 h. Aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The organic layer was dried and concentrated. The residue was purified by silica gel column chomatography (eluent, dichloromethane:methanol=15:1) and recrystallized from ethyl acetate to give the title compound (1.15 g) as a colorless solid.

Workup

  1. temperaturecooled to −78° C. again
  2. temperaturethe mixture was heated from −78° C. to room temperature
  3. stirringfurther stirred at room temperature for 24 h
  4. extractionthe mixture was extracted with ethyl acetate
  5. customThe organic layer was dried
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chomatography (eluent, dichloromethane:methanol=15:1)
  8. customrecrystallized from ethyl acetate

Sources & evidence

ORD record
ord-65a646e8874844b48093ebae130913d2
Source dataset
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06518257B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes