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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62798Erstellt: 24. Oktober 2026

Ethyl bromoacetate → Ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate

https://huagongshe.com/de/reaction/62798

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 2-oxocyclopentanecarboxylateHCID 69136—
LösungsmittelAcetoneHCID 180—
ProduktEthyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylateHCID 441864037,8%

Reaktionsbedingungen

Temperatur56 °C

Reaktionsschritte

To a solution of ethyl 2-oxocyclopentanecarboxylate (93.27 g, 597 mmol) and ethyl 2-bromoacetate (144.64 g, 866 mmol) in acetone (1.2 L) was added K2CO3 (165 g, 1194 mmol). The mixture was heated at 56° C. for 24 h. The solid was filtered off and the filter cake was washed with acetone (3×100 mL). The filtrate was concentrated and the resultant liquid was purified by a silica gel plug to give the title compound as light yellow liquid (54.7 g). LCMS m/z=243.3 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.23 (t, J=7.14 Hz, 3H), 1.24 (t, J=7.14 Hz, 3H), 1.95-2.03 (m, 1H), 2.06-2.15 (m, 2H), 2.35-2.50 (m, 2H), 2.55-2.60 (m, 1H), 2.80 (dd, J=15.2, 2.09 Hz, 1H), 2.95 (dd, J=15.2, 2.09 Hz, 1H), 4.09 (q, J=7.14 Hz, 2H), 4.12 (q, J=7.14 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447041B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-674f708676264ace99cd63176b38c8a3
Quellennotizuspto-grants-2016_09