Sodium Hydroxide → HCID 21254478, compound

HRID 439594Notes

Reaction equation

HRID 439594 reaction equation
C1(C(C2C=CC=CC=2)[N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)C=CC=CC=1.[OH-].[Na+].[ClH:22].C1(C2NC(C)=C(C([Cl:36])C)N=2)C=CC=CC=1>C(O)C.O>[ClH:36].[ClH:22].[ClH:36].[NH:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 70048BenzhydrylpiperazineHCID 22411958HCID 22411958, compound

Product 1

HCID 21254478HCID 21254478, compoundYield 55%

Reagents, catalysts & solvents 1

HCID 19096565Water ethanolSolvent2×

Procedure

14 Grams (0.052 mol) of N-(diphenylmethyl)piperazine and 6 grams (0.15 mol) of sodium hydroxide were dissolved in 180 ml of a mixture of ethanol :water 60:40. The mixture was heated to reflux, then 2-phenyl-4-(1-chloroethyl)-5-methylimidazole hydrochloride in 180 milliliters of ethanol:water 60:40 were added dropwise. After 4 to 5 hours under reflux, the reaction mixture was allowed to cool to room temperature. The oil that separated was washed twice with water, then dissolved in ether and hydrochloric acid was added. The precipitate was recrystallized from ethanol to give 1-diphenylmethyl-4- 1-(2-phenyl-5-methyl-1H-imidazol-4-yl)ethyl!piperazine trihydrochloride (55% yield), which melted at 215° C.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux
  3. temperatureAfter 4 to 5 hours under reflux
  4. customThe oil that separated
  5. washwas washed twice with water
  6. dissolutiondissolved in ether
  7. additionhydrochloric acid was added
  8. customThe precipitate was recrystallized from ethanol
  9. customto give 1-diphenylmethyl-4- 1-(2-phenyl-5-methyl-1H-imidazol-4-yl)ethyl

Sources & evidence

ORD record
ord-c44ee855069245c6a05b3eed63c9cb3c
Source dataset
uspto-grants-1996_05
Patent number
US05514800

Reaction notes

Loading…