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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369116Generated: November 1, 2026

3-Bromothiophene → HCID 18518623, compound

https://huagongshe.com/reaction/1369116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromothiopheneHCID 13383—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10958318HCID 10958318—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18518623HCID 1851862399%

Reaction Steps

To 3-bromothiophene (105.5 mg, 2.1 eq) in anhydrous THF (2 mL) under a nitrogen atmosphere and with stirring was added t-BuLi (0.38 mL, 2.1 eq, 1.7 M in pentane) at −40° C. (bath temperature). Stirring was continued for 30 minutes after which 1-(2-diethylaminoethyl)-4-bromoisatin (100.0 mg, 3.08×10−4 mol) in anhydrous THF (2 mL) was added dropwise. The resulting red colored solution was stirred at −40° C. for 8 hours. Saturated aqueous NH4Cl (1.5 mL) was added and the reaction mixture was allowed to warm to room temperature. The mixture was extracted with EtOAc and the combined extracts were dried (anhydrous Na2SO4). After filtration the solvent was removed in vacuo. Purification was carried out by column chromatography (silica gel, eluting 1% to 2% MeOH in CHCl3) to give the title compound as a light brown foam (124.5 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576656B1
Source datasetuspto-grants-2003_06
ORD IDord-31549d43439545a9baed87308b301e8c
Source noteuspto-grants-2003_06