Hydrochloric Acid → HCID 18418886, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([OH:10])=[O:9].[ClH:11].[CH3:12]O>>[ClH:11].[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([O:10][CH3:12])=[O:9]Participants
4
Procedure
A solution of 2-(2-pyridinyl)acetic acid (0.50 g, 3 mmol; prepared according to J. Prakt. Chem. 1961, 285, 118) in MeOH (20 mL) was saturated with HCl gas at 0° C., then was allowed to warm to RT. After stirring overnight, the reaction was concentrated under vacuum to afford the title compound (0.54 g, 100%) as a colorless solid: 1H NMR (CDCl3) δ8.90 (br s, 1H), 7.89 (m, 2H), 6.89 (t, J=6.5 Hz, 1H), 6.79 (d, J=8 Hz, 1H), 4.21 (m, 2H), 3.81 (s, 3H).
Workup
- concentrationthe reaction was concentrated under vacuum
Sources & evidence
- ORD record
- ord-fcfe33dd1c7d4666a3322414a1d8d086
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06458784B1
Reaction notes
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