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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393415Erstellt: 25. Oktober 2026

1,2-Dibromoethane → HCID 22660228, Verbindung

https://huagongshe.com/reaction/393415

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DibromoethaneHCID 7839—
EduktDiisopropylamineHCID 7912—
EduktHexaneHCID 8058—
EduktEthyl cyclopentanecarboxylateHCID 79550—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 22660228HCID 2266022880,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06806365B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-81055ff1f5a64e02a56c9eeb9591db73
Quellennotizuspto-grants-2004_10