Hydrochloric Acid → HCID 178489711, compound

HRID 2352635Notes

Reaction equation

HRID 2352635 reaction equation
C([O:3][C:4]([C:6]1[NH:10][N:9]=[C:8]([CH:11]=[CH:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[C:15]([O:20][CH3:21])[CH:14]=2)[CH:7]=1)=[O:5])C.[OH-].[K+].Cl>CCO.O>[CH3:21][O:20][C:15]1[CH:14]=[C:13]([CH:12]=[CH:11][C:8]2[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[NH:10][N:9]=2)[CH:18]=[CH:17][C:16]=1[OH:19]

Participants

6

Procedure

Ethyl-3-[β-(3-methoxy-4-hydroxyphenyl)ethenyl]-1H-pyrazole-5-carboxylate 0.49 g, 1.7 mmoles) is added to a solution of KOH (0.38 g, 6.8 mmoles) in 50 ml EtOH. The reaction is warmed to reflux overnight. After cooling to room temperature, the reaction is diluted to 200 ml with H2O, and acidified to pH=4 with HCl. A white precipitate forms, and it is collected by filtration. Drying in vacuum in the presence of P2O5 gives 0.3 g (68%) of the desired product, mp=270°-271° C. (dec).

Workup

  1. temperatureThe reaction is warmed
  2. temperatureto reflux overnight
  3. filtrationA white precipitate forms, and it is collected by filtration
  4. dry with materialDrying in vacuum in the presence of P2O5

Sources & evidence

ORD record
ord-1ea23c74f7f74dbc9e7c7191140a4351
Source dataset
uspto-grants-1989_10
Patent number
US04877881

Reaction notes

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