Sodium Hydroxide → HCID 67793757, compound
Reaction equation
[C:1]1([C:7]2[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:10]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[N:9]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][C:31]([O:33]CC)=[O:32])[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>CO>[OH2:32].[C:1]1([C:7]2[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:10]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:9]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][C:31]([OH:33])=[O:32])[N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of ethyl 3,4,5-triphenyl-lH-pyrazol-1-octanoate (3 g, 6.4 mmol), 3 N aqueous sodium hydroxide solution (6.4 mL, 19 mmol) and methanol (40 mL) was heated on a steam bath for 25 minutes before being cooled and concentrated in vacuo. The residue was diluted with water (25 mL) and 2 N hydrochloric acid solution added until pH =1. The mixture was extracted with dichloromethane and the combined extracts washed with water and saturated NaCl solution before being dried over sodium sulfate. Removal of the solvent left an oil that slowly crystallized. Recrystallization from a mixture of hexane and dichloromethane (2:1) afforded 3,4,5-triphenyl-lH-pyrazol1-octanoic acid hydrate (1.19 g, 42%); m.p. =97.5°-99.5° C. MS(CI): m/e =439 (MH+).
Workup
- temperaturewas heated on a steam bath for 25 minutes
- temperaturebefore being cooled
- concentrationconcentrated in vacuo
- additionThe residue was diluted with water (25 mL) and 2 N hydrochloric acid solution
- additionadded until pH =1
- extractionThe mixture was extracted with dichloromethane
- washthe combined extracts washed with water and saturated NaCl solution
- dry with materialbefore being dried over sodium sulfate
- customRemoval of the solvent
- waitleft an oil that
- customslowly crystallized
- customRecrystallization
- additionfrom a mixture of hexane and dichloromethane (2:1)
Sources & evidence
- ORD record
- ord-70c74f13fd5942c1b51064f413f1b482
- Source dataset
- uspto-grants-1991_02
- Patent number
- US04994482
Reaction notes
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