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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780788Generated: November 3, 2026

Hydrogen Bromide → 2-Bromo-6-methoxy-1,3-benzothiazole

https://huagongshe.com/reaction/1780788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2-Amino-6-methoxybenzothiazoleHCID 15630—
ReactantSodium NitriteHCID 23668193—
Catalystcopper(I) bromideHCID 24593—
SolventWaterHCID 962—
Product2-Bromo-6-methoxy-1,3-benzothiazoleHCID 11218765—

Reaction Conditions

Temperature0 °C

Reaction Steps

[(2-(6-Methoxybenzothiazolyl))carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester ##STR32## Slurry 2-amino-6-methoxybenzothiazole (0.255 mol) in water (325 mL), heat to reflux and add 48% hydrobromic acid (130 mL). Maintain at reflux for 20 minutes, cool to 0° C. and add a solution of sodium nitrite (17.56 g, 0.255 mol) in water (90 mL), maintaining a temperature of 0° C. Stir at 0° C. for 15 minutes and add by dropwise addition (while keeping cold) to a rapidly stirring mixture of copper (I) bromide (42.03 g,0.293 mol) in 48% hydrobromic acid (86 mL) and water (225 mL). Stir at room temperature for 20 minutes. Allow to stand overnight, extract into methylene chloride and dry (MgSO4). Evaporate the solvent in vacuo and purify by chromatography to give 2-bromo-6-methoxybenzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631268
Source datasetuspto-grants-1997_05
ORD IDord-c442cb7f99a64365b3e5f35265fe51ee
Source noteuspto-grants-1997_05