Imidazole → HCID 13269112, compound

HRID 1648750Notes

Reaction equation

HRID 1648750 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[O:17][CH:9]1[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[Cl:16].[NH:18]1[CH:22]=[CH:21][N:20]=[CH:19]1>O>[OH:17][CH:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[Cl:1])[CH:9]([N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[Cl:16]

Participants

4

Reactant 2

HCID 795ImidazoleHCID 3009192,3-bis(2-chlorophenyl)oxirane

Product 1

HCID 13269112HCID 13269112, compoundYield 86.8%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of 11 g (0.04 m) of 2,2'-dichloro-α,α'-epoxybibenzyl and 15 g (0.22 m) of imidazole is heated at 160° for 11/2 hours. The reaction is cooled, diluted with water, and extracted with ether. The combined ether extracts are washed with water, then saturated sodium chloride solution, and dried over MgSO4. Solvent is evaporated to give 12 g of a gummy solid, mp 62°-68°.

Workup

  1. temperatureis heated at 160° for 11/2 hours
  2. temperatureThe reaction is cooled
  3. extractionextracted with ether
  4. washThe combined ether extracts are washed with water
  5. dry with materialsaturated sodium chloride solution, and dried over MgSO4
  6. customSolvent is evaporated

Sources & evidence

ORD record
ord-fc1e1e8f49d54d999cc857014546529a
Source dataset
uspto-grants-1983_11
Patent number
US04413003

Reaction notes

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