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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619261Generated: October 30, 2026

Methyl iodide → 5-Bromo-2-(methylthio)benzo[d]thiazole

https://huagongshe.com/reaction/1619261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantHCID 178527757HCID 178527757—
SolventEthanolHCID 702—
Product5-Bromo-2-(methylthio)benzo[d]thiazoleHCID 280127180%

Reaction Steps

To a solution of 5-bromobenzo[d]thiazole-2-thiol (24 mg, 0.098 mmol) in EtOH (1.5 mL) was added triethylamine (10 mg, 0.098 mmol) and methyliodide (14 mg, 0.098 mmol). The mixture was heated at reflux for 1.5 h. Then the mixture was extracted with dichloromethane (3×10 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated to give 5-bromo-2-(methylthio)benzothiazole 20 mg (80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772285B2
Source datasetuspto-grants-2014_07
ORD IDord-0fd5e26727fa4100a1249daf4ff7215e
Source noteuspto-grants-2014_07