Hydrochloric Acid → HCID 15672407, compound
Reaction equation
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[C:8]([C:16]([O:18]C)=[O:17])[C:9]([C:12]([O:14]C)=[O:13])=[N:10][CH:11]=1.[OH-].[K+].Cl>CO>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[C:8]([C:16]([OH:18])=[O:17])[C:9]([C:12]([OH:14])=[O:13])=[N:10][CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 62 °C
Procedure
5-(1,3-Dioxolan-2-yl)-2,3-pyridinedicarboxylic acid, dimethyl ester (2.86 g, 0.011 mol) in methanol is added dropwise to a mixture of potassium hydroxide (1.26 g, 0.022 mol) and methanol. The reaction mixture is heated for 3 hours and 30 minutes at about 62° C., cooled to room temperature, acidified to pH 1 with concentrated hydrochloric acid, filtered through diatomaceous earth and the filtrate is concentrated in vacuo to yield the title compound as a pale yellow powder (2.86 g, 100%), identified by IR and NMR spectral analyses.
Workup
- temperaturecooled to room temperature
- filtrationfiltered through diatomaceous earth
- concentrationthe filtrate is concentrated in vacuo
Sources & evidence
- ORD record
- ord-05c5555588054b03a354038b820e2543
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05405827
Reaction notes
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