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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427355Generated: October 31, 2026

Hydrochloric Acid → 2-Chloro-6-trifluoromethylbenzothiazole

https://huagongshe.com/reaction/2427355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4-trifluoromethylanilineHCID 162001—
ReactantPotassium ethylxanthateHCID 2735045—
SolventDimethylformamideHCID 6228—
Product2-Chloro-6-trifluoromethylbenzothiazoleHCID 1147041999%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2-chloro-4-trifluoromethylaniline (15.0 g, 76.7 mmol) and potassium O-ethyl dithiocarbonate (29.5 g, 184.1 mmol) in 75 mL anhydrous DMF was heated at 130° C. overnight under a nitrogen atmosphere. The reaction mixture was cooled to rt, and then 1 N HCl solution (200 mL) was added with stirring to induce precipitation. After the mixture was stirred for 30 minutes, the solid precipitate was collected by filtration and rinsed with water. The filter cake was dissolved in 100 mL EtOAc, and the solution was dried over Na2SO4. EtOAc was removed by rotary evaporation, and the residue was dried in vacuo to afford the desired product as a white solid (18.0 g, 99%). 1H NMR (DMSO-d6) δ 14.00 (bs, 1 H), 8.20 (s, 1 H), 7.70 (d, 1 H), 7.40 (d, 1 H); GC-EIMS m/z 235 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968576B2
Source datasetuspto-grants-2011_06
ORD IDord-5b677918abe9461c9c5df4fd50a982b9
Source noteuspto-grants-2011_06