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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282588Generated: October 27, 2026

1,2-Dibromoethane → Ethyl 1-(2-bromoethyl)cyclopentanecarboxylate

https://huagongshe.com/reaction/1282588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
ReactantEthyl cyclopentanecarboxylateHCID 79550—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-(2-bromoethyl)cyclopentanecarboxylateHCID 2266022880.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice cold solution of diisopropylamine (56 mL, 0.396 mol) in THF 85 (mL) was added n-butyl lithium in hexane solution (240 mL, 1.6 M, 0.393 mol) over 20 min. The mixture was stirred at 0° C. for 30 min, cooled to a bath temperature of −65° C. and ethyl cyclopentane carboxylate (37.4 g, 0.263 mol) in THF (50 mL) was added over 20 min. After 1 hr, a solution of 1,2-dibromoethane (47 mL, 0.545 mol) in THF (50 mL) was added, the mixture was held at −65° C. for 3 hr and allowed to warm to room temperature overnight. The reaction was quenched by addition of saturated ammonium chloride solution (200 mL), the layers were separated and the aqueous layer was extracted with ethyl acetate (100 mL). The combined extracts were washed with 1:1 brine:water (250 mL) and were dried (Na2SO4). The solution was filtered and concentrated, diluted with toluene (100 mL) and concentrated. The dilution and concentration was repeated twice to give ethyl 1-(2-bromoethyl)cyclopentane carboxylate (52.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455550B1
Source datasetuspto-grants-2002_09
ORD IDord-86ba622cbc9347eeb146a920894b3f65
Source noteuspto-grants-2002_09