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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30891Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-6-trifluoromethylbenzothiazole

https://huagongshe.com/reaction/30891

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, 1H), 8.20 (s, 1H), 7.70 (d, 1H), 7.40 (d, 1H); GC-EIMS m/z 235 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423156B2
Source datasetuspto-grants-2008_09
ORD IDord-271aedb946a045a0bdfcbdee70c87dee
Source noteuspto-grants-2008_09