HCID 21393810, compound → HCID 21393805, compound

HRID 461505Notes

Reaction equation

HRID 461505 reaction equation
[Cl:1][C:2]1[C:3]([O:13]C)=[CH:4][CH:5]=[C:6]2[C:11]=1[CH:10]=[N:9][CH:8]=[C:7]2[CH3:12]>Br>[ClH:1].[Cl:1][C:2]1[C:3]([OH:13])=[CH:4][CH:5]=[C:6]2[C:11]=1[CH:10]=[N:9][CH:8]=[C:7]2[CH3:12]

Participants

3

Procedure

8-Chloro-7-methoxy-4-methylisoquinoline (0.89 g.) in 48% hydrobromic acid is refluxed for 48 hours. The mixture is evaporated to dryness in vacuo, redissolved in water and neutralized with ammonium hydroxide. The mixture is cooled and the precipitate is filtered off and treated with hydrogen chloride in ethanol. Ether is added and the precipitate is filtered off to give 8-chloro-7-hydroxy-4-methylisoquinoline hydrochloride.

Workup

  1. customThe mixture is evaporated to dryness in vacuo
  2. dissolutionredissolved in water and neutralized with ammonium hydroxide
  3. temperatureThe mixture is cooled
  4. filtrationthe precipitate is filtered off
  5. additiontreated with hydrogen chloride in ethanol
  6. additionEther is added
  7. filtrationthe precipitate is filtered off

Sources & evidence

ORD record
ord-70c4f6521bdd44ffb4097dbb0b1b8683
Source dataset
uspto-grants-1977_12
Patent number
US04062961

Reaction notes

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