Imidazole → 4-(2-Imidazolylacetyl)benzenecarbonitrile

HRID 1823428Notes

Reaction equation

HRID 1823428 reaction equation
Cl[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]#[N:12])=[CH:7][CH:6]=1)=[O:4].[NH:13]1[CH:17]=[CH:16][N:15]=[CH:14]1>CC#N.ClCCl.O>[NH:13]1[CH:17]=[CH:16][N:15]=[C:14]1[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]#[N:12])=[CH:7][CH:6]=1)=[O:4]

Participants

6

Reactant 2

HCID 795ImidazoleHCID 142493Benzonitrile, 4-(chloroacetyl)-

Product 1

HCID 221429994-(2-Imidazolylacetyl)benzenecarbonitrileYield 90%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 6342AcetonitrileSolventHCID 6344DichloromethaneSolvent

Procedure

A stirred solution of 4-(2-chloroacetyl)benzenecarbonitrile (0.5 M) and imidazole (1.5 M) in CH3CN (200 ml) were heated for 14 hours at 60° C. The product was stripped of solvent under reduced pressure. The residue was diluted with dichloromethane (250 ml) and water (100 ml), and the mixture was stirred for 30 min. After filtering off a solid impurity, the aqueous layer was removed and discarded. The organic layer was washed sequentially with water (60 ml), sat. aq. NaHCO3 (60 ml), water (60 ml), brine (60 ml), dried with Na2SO4, filtered, and concentrated under reduced pressure. The dark colored oil was dried overnight in vacuo giving 4-(2-imidazolylacetyl)benzenecarbonitrile in 90% yield.

Workup

  1. filtrationAfter filtering off a solid impurity
  2. customthe aqueous layer was removed
  3. washThe organic layer was washed sequentially with water (60 ml), sat. aq. NaHCO3 (60 ml), water (60 ml), brine (60 ml)
  4. dry with materialdried with Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe dark colored oil was dried overnight in vacuo

Sources & evidence

ORD record
ord-19d27aac3c994f0091a1de73f8a1db05
Source dataset
uspto-grants-2006_05
Patent number
US07037918B2

Reaction notes

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