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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220489Erstellt: 24. Oktober 2026

Ethyl bromoacetate → Ethyl 4-oxo-3-propanoylhexanoate

https://huagongshe.com/de/reaction/220489

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktSodium hydrideHCID 24758—
Edukt3,5-HeptanedioneHCID 81923—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 4-oxo-3-propanoylhexanoateHCID 5098800477%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Dissolve heptane-3,5-dione (2.5 g, 19.5 mmol) in dry tetrahydrofuran (10 mL) and add the resulting solution dropwise to a chilled (0° C.) suspension of sodium hydride (0.94 g, 23.4 mmol, 60% dispersion in oil) in tetrahydrofuran (20 mL). Stir at 0° C. for 1 hr., then add bromoacetic acid ethyl ester (2.6 mL, 23.4 mmol) dropwise. Stir for 16 hr. at 0° C. and warm to room temperature. Partition the reaction mixture between diethyl ether (100 mL) and saturated aqueous ammonium chloride solution (50 mL). Separate the organic layer and wash with saturated aqueous sodium chloride solution (50 mL), dry (sodium sulfate), filter and concentrate. Purify using silica gel chromatography, eluting with 10:1 hexanes:ethyl acetate, to give 4-oxo-3-propionyl-hexanoic acid ethyl ester as an oil (3.2 g, 77%). 1H-NMR (400 MHz, CDCl3) δ 4.08 (m, 3H), 2.83 (d, 2H), 2.55 (q, 2H), 1.21 (t, 3H), 1.02 (t, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202873B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-e5cf9ef8eeba4791a5c43d82a63ad79c
Quellennotizuspto-grants-2012_06