Ethyl Bromide → HCID 86719636, compound

HRID 922634Notes

Reaction equation

HRID 922634 reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[Cl:7].[OH-].[K+].[Br:10][CH2:11][CH3:12].[K+].[Br-].BrCC[C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1>C(#N)C>[Br-:10].[CH2:26]([N+:3]1[C:2]([Cl:1])=[C:6]([Cl:7])[N:5]([C:26]2[C:27]3[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:23]=[CH:24][C:25]=2[CH2:11][CH3:12])[CH:4]=1)[CH2:27][CH2:18][CH2:19][CH2:20][CH3:21]

Participants

7

Reactant 5

HCID 6332Ethyl BromideHCID 14797Potassium HydroxideHCID 1395411-(2-Bromoethyl)naphthaleneHCID 1400184,5-DichloroimidazoleHCID 253877Potassium Bromide

Product 1

HCID 86719636HCID 86719636, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

4,5-Dichloroimidazole (1.23 g, 9 mmol) will be dissolved into acetonitrile. Potassium hydroxide (0.61 g, 9.9 mmol) will be added and the mixture will be allowed to stir for 0.5 h. 1-bromethane (9 mmol) will be added and the solution will be allowed to reflux overnight. The solution will be filtered hot to remove a white precipitate (presumed to be KBr) and 1-(2-bromoethyl)naphthalene (9 mmol) will be added and the mixture will be returned to reflux overnight. The mixture will be allowed to cool to room temperature, and the volatiles will be removed en vacuo resulting in the product.

Workup

  1. temperatureto reflux overnight
  2. filtrationThe solution will be filtered hot
  3. additionwill be added
  4. temperatureto reflux overnight
  5. customthe volatiles will be removed en vacuo
  6. customresulting in the product

Sources & evidence

ORD record
ord-1a1f856e239244b5ac3cc5a5e2b81ba8
Source dataset
uspto-grants-2016_03
Patent number
US09278951B2

Reaction notes

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