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ChemicalBook CAS DataBase List 3-Chloro-1,2-benzisothiazole
7716-66-7

3-Chloro-1,2-benzisothiazole synthesis

13synthesis methods
1,2-Benzisothiazol-3(2H)-one

2634-33-5

3-Chloro-1,2-benzisothiazole

7716-66-7

Example 1A: To a 1 L four-necked round-bottomed flask equipped with a mechanical stirrer, a thermometer and a reflux condenser tube were sequentially added 75.6 g (0.5 mol) of 1,2-benzisothiazol-3-one, 54.8 g (0.75 mol) of N,N-dimethylformamide (DMF) and 100.0 g of chlorobenzene as a solvent. Stirring was turned on and the temperature of the reaction system was maintained between 70 °C and 80 °C, followed by the slow dropwise addition of 71.4 g (0.6 mol) of thionyl chloride (SOCl2) over a period of 1 hour. After the dropwise addition was completed, the reaction mixture was kept at the same temperature and the reaction was continued with stirring for 8 hours. Upon completion of the reaction, the liquid reaction mixture was concentrated under reduced pressure to remove the solvent and unreacted thionyl chloride. The resulting crude product was subjected to decompression distillation at 128 °C under reduced pressure at 0.93 kPa to yield 75.1 g (0.45 mol) of the target product 3-chloro-1,2-benzisothiazole in 90% yield as 1,2-benzisothiazol-3-one.

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Yield:7716-66-7 92.7%

Reaction Conditions:

in chlorobenzene;paraffin oil

Steps:

6 Example 6
Example 6 Example 5 was repeated, except that 4 kg of 93% by weight pure benzisothiazolone and 90 g of 1,3-dimethylimidazolidinone in 5 l of chlorobenzene were phosgenated. To obtain the reaction product, 200 ml of high boiling paraffin oil were added prior to the vacuum distillation, and a Vigreux column of 20 cm in length was used. 3-Chlorobenzisothiazole of a purity of 99.4% by weight was obtained in a yield of 92.7% of theory.

References:

Bayer Aktiengesellschaft US5883258, 1999, A

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