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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785762Generated: October 26, 2026

Methyl iodide → 5-Bromo-2-ethyl-1,3-benzothiazole

https://huagongshe.com/reaction/1785762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactant5-Bromo-2-methylbenzothiazoleHCID 3017457—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-ethyl-1,3-benzothiazoleHCID 22730220—

Reaction Steps

A 0° C. solution of diisopropylamine (340 μL, 2.41 mmol) in THF (3 mL) was treated with 2.5M n-butyllithium in hexanes (0.88 mL), stirred for 20 minutes, added to a −78° C. solution of 5-bromo-2-methyl-1,3-benzothiazole (250 mg, 1.10 mmol) in THF (3 mL), stirred for 30 minutes, treated with iodomethane (340 μL, 5.50 mmol), and stirred for 1 hour. The mixture was diluted with ethyl acetate (50 mL), washed sequentially with 1M HCl (5 mL), water (5 mL), and brine (5 mL), dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 30% hexanes/dichloromethane to provide the desired product. MS (DCI) m/e 242 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504512B2
Source datasetuspto-grants-2009_03
ORD IDord-794ece45b1d0482a85885c6158392336
Source noteuspto-grants-2009_03