3,5-Dichloro-2-(trichloromethyl)pyridine → Pyridine, 2,3,5-trichloro-
Reaction equation
[Cl:1][C:2]1[C:3](C(Cl)(Cl)Cl)=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=1.[Cl:13]Cl>>[Cl:13][C:3]1[C:2]([Cl:1])=[CH:7][C:6]([Cl:8])=[CH:5][N:4]=1Participants
Procedure
The batch chlorinator R1 was charged with 50 grams of starting material containing 90.4% 3,5-dichloro-2-trichloromethyl pyridine by weight, and chlorine was sparged through the reactor by means of sparger 14 for 15 hours at a reaction temperature of 170° C. Samples were taken at the time which corresponded to about 14% conversion of the 3,5-dichloro-2-trichloromethly pyridine. The yield of 2,3,5-trichloropyridine at this temperature, was about 14%, i.e., about half the yield of like runs at 200° C. (Table ONE). The chlorination was then continued under the same reaction conditions except at a temperature of 160° C. and yielded no appreciable quantity of 2,3,5-trichloropyridine in 8 hours. Analytical data with respect to this Example are presented in the following Table TWO:
Workup
- customwas sparged through the reactor by means of sparger 14 for 15 hours at a reaction temperature of 170° C
- customat 200° C.
- customThe chlorination was then continued under the same reaction conditions except at a temperature of 160° C.
Sources & evidence
- ORD record
- ord-436e12bdfbd24b82ad7a2e007161da74
- Source dataset
- uspto-grants-1986_01
- Patent number
- US04563531
Reaction notes
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