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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9575Generated: October 25, 2026

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

https://huagongshe.com/reaction/9575

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 numberUS07091228B2
Source datasetuspto-grants-2006_08
ORD IDord-d12c540085124d09aa48e1da1b1b4a13
Source noteuspto-grants-2006_08