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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82754Generated: October 26, 2026

Cyanoacetic acid → 6-(5-Bromothiophen-2-yl)-3,6-dioxohexanenitrile

https://huagongshe.com/reaction/82754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-(5-Bromo-2-thienyl)-4-oxobutyric acidHCID 11184604—
SolventTetrahydrofuranHCID 8028—
Product6-(5-Bromothiophen-2-yl)-3,6-dioxohexanenitrileHCID 5829764669%

Reaction Steps

To a solution of 2-cyanoacetic acid (13 g, 50 mmol) in THF (100 mL) was added dropwise i-PrMgC1 (16 g, 250 mmol) at −78° C. for 1 h. A solution of 4-(5-bromothiophen-2-yl)-4-oxobutanoic acid (8A) and CDI (12 g, 74 mmol) in THF was added dropwise at −78° C. and the resultant mixture was stirred at −78° C. for 1 h and at room temperature for 1 h. The reaction mixture was quenched with saturated ammonium chloride (200 mL). The organic phase was separated, dried over Na2SO4, filtered, concentrated and purified by silica gel column chromatography (PE:EA=5:1) to afford 8B as a black oil (9.7 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846736B2
Source datasetuspto-grants-2014_09
ORD IDord-f6bce802f1ca45b3890a0ff1243aa489
Source noteuspto-grants-2014_09