3,5-Dichloro-2-(trichloromethyl)pyridine → Pyridine, 2,3,5-trichloro-

HRID 1284595Notes

Reaction equation

HRID 1284595 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]=1

Participants

3

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

  1. customwas sparged through the reactor by means of sparger 14 for 15 hours at a reaction temperature of 170° C
  2. customat 200° C.
  3. 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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