Nicotinic Acid → 3-Pyridinecarbonyl chloride, hydrochloride (1:1)
Reaction equation
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.S(Cl)([Cl:12])=O>>[ClH:12].[C:1]([Cl:12])(=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1Participants
3
Procedure
To nicotinic acid (41 g, 0.333 mol) at 0° C. was added thionyl chloride (115 ml, 1.58 mol) with stirring. The mixture was refluxed for one hour, and the white crystalline product was filtered and washed sparingly with dry benzene. Excess thionyl chloride was azeotroped off with dry benzene immediately before use. Yield 90% (53.97 g) of nicotinoyl chloride hydrochloride; NMR, IR identical with literature values.
Workup
- temperatureThe mixture was refluxed for one hour
- filtrationthe white crystalline product was filtered
- washwashed sparingly with dry benzene
- customExcess thionyl chloride was azeotroped off with dry benzene immediately before use
Sources & evidence
- ORD record
- ord-d4ad703b072c42d98fe45b4151b56bac
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04617298
Reaction notes
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