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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261885Generated: November 1, 2026

1,4-Dibromobutane → Diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate

https://huagongshe.com/reaction/2261885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantDiethyl 5-(cyanomethyl)benzene-1,3-dioateHCID 59709094—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioateHCID 67318465—

Reaction Steps

To a solution of diethyl 5-(cyanomethyl)benzene-1,3-dioate (500 mg, 1.9 mmol) in 18.6 mL THF was added potassium bis(trimethylsilyl)amide (1.1 g, 5.7 mmol) and the reaction was stirred at rt for 5 min. 1,4-Dibromobutane (0.25 mL, 2.1 mmol) was added, the mixture was stirred for 45 min and then quenched with 1N HCl. Ethyl acetate was added, the layers separated and the organic layer washed with water and brine. Drying, solvent evaporation and flash chromatography (silica gel, 0->15% EtOAc/hexanes) gave diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate. 1H NMR (400 MHz, CDCl3) δ 8.63 (m, 1H), 8.31 (m, 2H), 4.43 (q, J=7.1 Hz, 4H), 2.56 (m, 2H), 2.14-1.99 (m, 6H), 1.43 (t, J=7.1 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07847100B2
Source datasetuspto-grants-2010_12
ORD IDord-30ff04dc20044f1baf812ddc82bc8df4
Source noteuspto-grants-2010_12