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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427354Generated: November 4, 2026

Sulfuryl chloride → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/2427354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant5-(trifluoromethyl)-1,3-benzothiazole-2-thiolHCID 178419087—
Product2-Chloro-5-(trifluoromethyl)-1,3-benzothiazoleHCID 2198584994%

Reaction Steps

Sulfuryl chloride (9.09 g, 67.33 mmol) was added with stirring to 2-mercapto-5-(trifluoromethyl)benzothiazole (2.64 g, 11.22 mmol) over a period of 5 minutes. The reaction mixture was then allowed to stand for approximately 1 h. Ice water was added to the reaction mixture with stirring to decompose the excess of sulfuryl chloride, and the product was then extracted with ethyl acetate. The organic layer was washed with water (3×) and brine, dried over anhydrous Na2SO4 and concentrated. The resulting solid was dissolved in EtOAc and filtered though a short silica-gel column, eluting with EtOAc, to give 2-chloro-5-(trifluoromethyl)benzothiazole (2.50 g, 94%). LC-MS m/z 238.0 (MH+), ret. time 2.55 min; 1H NMR (400 MHz, DMSO-d6) δ 7.81 (d, 1H), 8.38 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968576B2
Source datasetuspto-grants-2011_06
ORD IDord-30bfbec4abc54052a08be4e3eac35233
Source noteuspto-grants-2011_06