Benzyl Bromide → HCID 20359956, compound

HRID 2082645Notes

Reaction equation

HRID 2082645 reaction equation
[OH:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[N:4]=[C:3]1[C:12]([F:15])([F:14])[F:13].[CH2:16](Br)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH2:16]([O:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[N:4]=[C:3]1[C:12]([F:15])([F:14])[F:13])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

5

Procedure

1-Hydroxy-6-chloro-2-(trifluoromethyl)-1H-imidazo-(4,5-b)pyridine (5 grams), 10 milliliters of benzyl bromide, 20 grams of anhydrous potassium carbonate, and 100 milliliters of ethanol were mixed, heated to reflux, and refluxed for one hour. The reaction mixture was then filtered, evaporated under vacuum, and extracted with diethyl ether. The extract was filtered and evaporated under vacuum yielding a dark oil which on standing crystallized as the desired 1-benzyloxy-6-chloro-2-(trifluoromethyl)- 1H-imidazo(4,5-b)pyridine. It was recrystallized from a mixture of acetone and petroleum ether boiling at 60°-80° C., m.p., 107°-09° C.

Workup

  1. temperatureheated
  2. temperatureto reflux
  3. temperaturerefluxed for one hour
  4. filtrationThe reaction mixture was then filtered
  5. customevaporated under vacuum
  6. extractionextracted with diethyl ether
  7. filtrationThe extract was filtered
  8. customevaporated under vacuum
  9. customyielding a dark oil which
  10. customon standing crystallized as the desired 1-benzyloxy-6-chloro-2-(trifluoromethyl)- 1H-imidazo(4,5-b)pyridine
  11. customIt was recrystallized from a mixture of acetone and petroleum ether boiling at 60°-80° C., m.p., 107°-09° C

Sources & evidence

ORD record
ord-02502fe986c24c99a467aa419afc0794
Source dataset
uspto-grants-1978_04
Patent number
US04082534

Reaction notes

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