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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341976Generated: October 26, 2026

Benzisothiazole → 3-Chloro-1,2-benzisothiazole

https://huagongshe.com/reaction/341976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzisothiazoleHCID 9225—
ReactantThionyl ChlorideHCID 24386—
ReactantChlorineHCID 24526—
Reactant2-(Methylthio)benzaldehyde oximeHCID 786757—
SolventChlorobenzeneHCID 7964—
Product3-Chloro-1,2-benzisothiazoleHCID 59819096.1%

Reaction Steps

In a 300 ml four-necked flask equipped with a stirrer, a thermometer, and a condenser, 100 g of monochlorobenzene was placed in advance, to which 33.4 g (0.2 mol) of 2-(methylthio)benzaldehyde oxime was added under nitrogen atmosphere. 25.2 g (0.21 mol) Of thionyl chloride was added dropwise thereto while stirring at a temperature of from -10° to -15° C. and allowed to react for 1 hour at the same temperature. After the termination of the reaction, 15.6 g (0.22 mol) of chlorine was continuously blown into the reaction mixture containing 1,2-benzisothiazole while stirring at a temperature of from 70° to 80° C. and allowed to react for 1 hour at the same temperature. After the termination of the reaction, the reaction mixture was subjected to distilling off of the solvent and then to distillation under reduced pressure to give 32.6 g of 3-chloro-1,2-benzisothiazole. The yield was 96% to the 2-(methylthio)benzaldehyde oxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856504
Source datasetuspto-grants-1999_01
ORD IDord-5452ffc334694ae09b9bc88857992547
Source noteuspto-grants-1999_01