Sodium Hydroxide → 3-Carboxy-1,4-dimethyl-5-(p-toluoyl)-pyrrole-2-acetic acid
Reaction equation
[CH3:1][N:2]1[C:6]([C:7]([C:9]2[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][CH:10]=2)=[O:8])=[C:5]([CH3:16])[C:4]([C:17]([O:19]CC)=[O:18])=[C:3]1[CH2:22][C:23]([O:25]CC)=[O:24].[OH-].[Na+]>>[C:17]([C:4]1[C:5]([CH3:16])=[C:6]([C:7]([C:9]2[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][CH:10]=2)=[O:8])[N:2]([CH3:1])[C:3]=1[CH2:22][C:23]([OH:25])=[O:24])([OH:19])=[O:18]Participants
3
Procedure
A suspension of 54 g. (0.145 mole) of ethyl 1,4-dimethyl-3-ethoxycarbonyl-5-(p-toluoyl)-pyrrole-2-acetate in 500 g. of 25% sodium hydroxide is heated at just below reflux for 3 hrs. The yellow suspension is then poured into ice-hydrochloric acid and the precipitated solid is collected, air dried and recrystallized from acetone-water to give 3-carboxy-1,4-dimethyl-5-(p-toluoyl)-pyrrole-2-acetic acid as a white solid, m.p. 229°-230° C.
Workup
- additionA suspension of 54 g
- temperaturebelow reflux for 3 hrs
- customthe precipitated solid is collected
- customair dried
- customrecrystallized from acetone-water
Sources & evidence
- ORD record
- ord-efe03058cf004107b6282009180a2566
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04070368
Reaction notes
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