Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926420Generated: October 31, 2026

Hydrochloric Acid → 2-Chloro-4,5-difluorobenzo[d]thiazole

https://huagongshe.com/reaction/1926420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium NitriteHCID 23668193—
Reactant4,5-Difluoro-1,3-benzothiazol-2-amineHCID 61075402—
CatalystCopper SulfateHCID 24462—
CatalystCuprous chlorideHCID 62652—
Product2-Chloro-4,5-difluorobenzo[d]thiazoleHCID 24728968—

Reaction Steps

To a mixture of 2-amino-4,5-difluoro-1,3-benzothiazole (130 mg, 0.70 mmol) and CuSO4 (20 mg) in conc. HCl (20 mL) was added NaNO2 (96 mg, 1.4 mmol, 2 eq, dissolved in 5 mL of water) dropwise at −10° C. over about 15 min. The reaction mixture was stirred for 1 h, poured into a solution of CuCl (67 mg, 0.7 mmol, 1 eq.) in conc. HCl (20 mL), and stirring was continued at ambient temp. for 30 min. The reaction mixture was extracted with diethyl ether (3×30 mL). The combined organic layers were washed with water (10 mL), dilute ammonium hydroxide (10 mL), brine (20 ml), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluted by 2% methanol in methylene chloride) to afford the title compound. 1H-NMR (CDCl3, 300 MHz): δ=7.20-7.15 (m, 1H), 7.13-7.04 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-c44c3fe62e3044c89dada64cd5ce1072
Source noteuspto-grants-2012_05