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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370495Generated: October 25, 2026

Hydrochloric Acid → 3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine

https://huagongshe.com/reaction/1370495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-DichlorobenzothiazoleHCID 77176—
Reactant4-Amino-2,6-dichlorophenolHCID 80037—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamineHCID 2214877649.3%

Reaction Conditions

Temperature160 °C

Reaction Steps

To the solution of 4-amino-2,6-dichloro phenol (6 g, 26.5 mmol) and 2,6-dichlorobenzothiazole (101) (6 g, 29.4 mmol, 1.1 equiv.) in DMSO (25 mL), was added K2CO3 (11 g, 80 mmol, 3.0 equiv.). The mixture was stirred and heated to 160° C. After 5.5 h water (20 mL) was added to the reaction mixture, which was neutralized with 2N HCl., and was extracted with AcOEt three times. And the organic layer was washed with brine and was dried over anhydrous MgSO4, and then concentrated. Crude residue was purified by column chromatography (CHCl3/acetone=9/1, 180 g of silica gel) to afford 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine (102) as a black solid (4.52 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583157B2
Source datasetuspto-grants-2003_06
ORD IDord-bf033d1d5294458c906b11d1d1b50641
Source noteuspto-grants-2003_06