Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664625Generated: November 1, 2026

Ammonia → 6-Bromo-1,3-benzothiazole

https://huagongshe.com/reaction/1664625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrogen BromideHCID 260—
Reactant6-AminobenzothiazoleHCID 68288—
ReactantSodium NitriteHCID 23668193—
Catalystcopper(I) bromideHCID 24593—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product6-Bromo-1,3-benzothiazoleHCID 2795171—

Reaction Steps

A solution of sodium nitrite (0.147 g, 2.1 mmol) in water (1.0 mL) was slowly added to a suspension of 6-aminobenzothiazole (0.30 g, 2.0 mmol) in HBr (48% in water, 3 mL) at 0° C. and then the mixture was stirred at room temperature for 30 min. The formed solution was then slowly added to a solution of copper (I) bromide (0.435 g, 3.0 mmol) in HCl (conc., 5 mL) at 0° C. After the addition, the mixture was stirred at 60° C. for 1.5 h. Cooled down, and the reaction mixture was basified with excess ammonia and extracted with diethyl ether. The combined extract was washed with water, brine, dried and concentrated. The 6-bromobenzothiazole (0.26 g) was obtained by Combiflash and then converted to the final compound using procedures analogous to those for example 1, MS(ESI): (M+H)+=413.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039471B2
Source datasetuspto-grants-2011_10
ORD IDord-45eba150728c454abf74e65a801d3069
Source noteuspto-grants-2011_10