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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487714Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/1487714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
ReactantPotassium ethylxanthateHCID 2735045—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(trifluoromethyl)-1,3-benzothiazoleHCID 21985849—

Reaction Steps

3-Amino-4-bromobenzotrifluoride (1.00 g, 4.17 mmol) and potassium ethyl xanthate (1.60 g, 10.0 mmol) were heated to 130° C. in DMF (5 mL) overnight. After cooling to rt, the reaction mixture was diluted with 1 M aqueous HCl (15 mL) and stirred at rt for an additional 30 min. The resulting solid was collected by filtration and washed with water (2×). The solid was dissolved in EtOAc, dried over Na2SO4, filtered, and concentrated under reduced pressure. This gave 0.895 g (91%) of the 2-mercapto intermediate as a yellow solid. LC-MS: RT=8.60 min., [M+H]+=236.2. The material was suspended in sulfuryl chloride (5 mL) and CH2Cl2(2 mL). After 2 h, water (20 mL) was added and stirring continued for an additional 30 min. The reaction mixture was extracted with EtOAc (3×), and the combined extracts were dried over Na2SO4, filtered, concentrated under reduced pressure. This gave 0.886 g (98%) of the title compound as an off-white solid. LC-MS: RT=10.12 min., compound does not ionize.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428522B2
Source datasetuspto-grants-2016_08
ORD IDord-ceff1fef3cff47dda5fcc5f31560fd23
Source noteuspto-grants-2016_08