Hydrochloric Acid → HCID 178526838, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[ClH:11]>O>[Cl:11][C:7]1[C:2]([OH:1])=[N:3][CH:4]=[C:5]([N+:8]([O-:10])=[O:9])[CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 5 L flask with mechanical stirrer, thermocouple, and addition funnel was charged with 2-hydroxy-5-nitropyridine (200 g,) and concentrated HCl (890 mL). The mixture was warmed to 50–55° C. and a solution of KClO3 (61.3 g, 0.5 mol) in water (850 mL) was added dropwise over 75 minutes maintaining the reaction temperature at 55–59° C. Following complete addition, the reaction mixture was cooled in an ice-water bath to an internal temperature of <6° C. and then filtered. The filter cake was washed with cold water (700 mL) and dried under vacuum at 50° C. for 12 hours to provide the title compound. 1H NMR (CDCl3, 300 MHz) δ 7.43 (d, J=3 Hz, 1H), 7.59 (d, J=3 Hz, 1H).
Workup
- additionA 5 L flask with mechanical stirrer, thermocouple, and addition funnel
- temperatureThe mixture was warmed to 50–55° C.
- temperaturemaintaining the reaction temperature at 55–59° C
- additionaddition
- temperaturethe reaction mixture was cooled in an ice-water bath to an internal temperature of <6° C.
- filtrationfiltered
- washThe filter cake was washed with cold water (700 mL)
- customdried under vacuum at 50° C. for 12 hours
Sources & evidence
- ORD record
- ord-a6b64e237640414db5e998021839d166
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07354937B2
Reaction notes
Loading…