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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847806Generated: October 26, 2026

1,2-Dichloroethane → 4-chloro-N-methylbenzothiazolone

https://huagongshe.com/reaction/847806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactant4-ChlorobenzothiazoloneHCID 53400688—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product4-chloro-N-methylbenzothiazoloneHCID 6964501093.9%

Reaction Steps

4-Chlorobenzothiazolone (9.28 g, 0.05 mole) was dissolved in a solution of sodium hydroxide (3.19 g, 0.075 mole) in water (500 ml), and tetra-n-butylammonium bromide (0.48 g, 0.0015 mole) and ethylene dichloride (300 ml) were added thereto. Dimethyl sulfate (9.40 g, 0.075 mole) was added dropwise thereto at room temperature, and the mixture was stirred at room temperature for 1 hour, followed by phase-separation. The ethylene dichloride layer was washed once with water, and the solvent was removed under reduced pressure to obtain 9.37 g of 4-chloro-N-methylbenzothiazolone as pale yellow crystals. Yield 93.9%, purity 98.7%, m.p. 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04293702
Source datasetuspto-grants-1981_10
ORD IDord-5d1e1d871b804ddda12daf9877af0ddf
Source noteuspto-grants-1981_10