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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519923Generated: November 3, 2026

1,4-Dioxane → 2-(4-Bromo-2-nitrothiophen-3-yl)thiazole

https://huagongshe.com/reaction/1519923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant3,4-Dibromo-2-nitrothiopheneHCID 1201506—
Reactant2-(Tributylstannyl)-1,3-thiazoleHCID 2763259—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product2-(4-Bromo-2-nitrothiophen-3-yl)thiazoleHCID 6875524185.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3,4-dibromo-2-nitrothiophene (242 mg, 0.85 mmol), 2-(tributylstannyl)thiazole (315 mg, 0.84 mmol), Pd(Ph3P)4 catalyst (194 mg, 0.17 mmol) and dioxane (0.9 mL) was heated in the microwave to 130° C. for 25 min. The reaction mixture was diluted with EtOAc and filtered to remove solids. The remaining organic solution was washed with saturated, aqueous solutions of sodium bicarbonate and salt before drying over sodium sulfate. The organic was concentrated under reduced pressure to give a dark oil. The crude product was purified by column chromatography (30% EtOAc/hexanes) to give 2-(4-bromo-2-nitrothiophen-3-yl)thiazole (210 mg). LCMS m/z of 289.1/291.1 with a retention time of 2.043 min on the [1] method.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-8286b25c748f453b9564fd2da27acab0
Source noteuspto-grants-2015_07