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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427286Generated: October 30, 2026

4-Methoxy-2-aminobenzothiazole → 2-Bromo-4-methoxy-1,3-benzothiazole

https://huagongshe.com/reaction/427286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-aminobenzothiazoleHCID 21622—
ReactantPotassium BromideHCID 253877—
ReactantSodium NitriteHCID 23668193—
SolventSulfuric AcidHCID 1118—
Product2-Bromo-4-methoxy-1,3-benzothiazoleHCID 1835699778.8%

Reaction Steps

To a solution of 2-amino-4-methoxybenzothiazole (1.5 g) and potassium bromide (3.5 g) in sulphuric acid (1.25M, 50 ml) at 0° C. was added sodium nitrite (0.86 g) over a period of 1 hr. The reaction was allowed to warm to room temperature and stirred for 2 hrs, before being extracted with dichloromethane (3×50 ml). The combined organic extracts were dried over magnesium sulphate (5 g), and the solvent removed in vacuo to yield an off white solid. This was purified by flash chromatography (eluent 50% ethyl acetate/hexane) to yield the title compound as a white solid (1.6 g). TLC Ff 0.30 (20% ethyl acetate in hexane)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313116B1
Source datasetuspto-grants-2001_11
ORD IDord-d1caa672c92a4f6d8821d2f04995a1c3
Source noteuspto-grants-2001_11