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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427236Generated: November 1, 2026

Diethyl Ether → 2,6-Dichlorobenzothiazole

https://huagongshe.com/reaction/2427236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium ChlorideHCID 5234—
Reactant6-Chloro-2-benzothiazolamineHCID 7226—
ReactantSodium NitriteHCID 23668193—
CatalystCupric ChlorideHCID 24014—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
SolventPhosphoric AcidHCID 1004—
Product2,6-DichlorobenzothiazoleHCID 7717648%

Reaction Steps

2-Amino-6-chlorobenzothiazole (15.7 g, 85 mmol) in H3PO4 (85%) (470 ml) was heated to 100 degrees and dissolved. Then clear solution was cooled and vigorously stirred by mechanical stirrer. NaNO2 (17.6 g, 255 mmol) in water (30 ml) was added slowly keeps the temperature below 0 degrees. Separately a solution of CuSO4/5H2O (85 g), NaCl (107 g) in water (350 ml) was cooled to −5 degrees and stirred by mechanical stirrer. After Potassium Iodide Starch paper's color was disappeared Diazonium solution was keeping cold and added slowly to the copper chloride solution with vigorous stirring. The reaction Mixture was allowed to warm to room temperature. After 1-hour water (1 L) and ether (1 L) were added to the reaction mixture and extracted twice. Organic layer was washed by water and dried over anhydrous MgSO4 and concentrated. Crude residue was purified by silica gel chromatography (H/A=4/1, 180 g of silica gel) to provide title compound 363 (7.46 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968567B2
Source datasetuspto-grants-2011_06
ORD IDord-7c7c8524ed084c9fa16cbc870a268216
Source noteuspto-grants-2011_06