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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519974Generated: November 2, 2026

2-Chloro-3-nitrothiophene → 1-Methyl-4-(3-nitrothiophen-2-yl)-1H-imidazole

https://huagongshe.com/reaction/1519974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-nitrothiopheneHCID 220186—
Reactant1-Methyl-4-(tributylstannyl)-1H-imidazoleHCID 21901141—
Product1-Methyl-4-(3-nitrothiophen-2-yl)-1H-imidazoleHCID 68784592—

Reaction Conditions

Temperature95 °C

Reaction Steps

The title compound was prepared from 2-chloro-3-nitrothiophene (2.57 g, 15.7 mmol) and 1-methyl-4-(tributylstannyl)-1H-imidazole (8.64 g, 23.3 mmol) using protocol E except the reaction was heated to 90° C. (rather than 95° C.) and was purified by flash chromatography (hexane:ethyl acetate). Method [1] Retention time 0.57 min by HPLC (MH+ 210).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-4770828d10bb4d8cabd4b8be49830a9e
Source noteuspto-grants-2015_07