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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 751439Erstellt: 26. Oktober 2026

Ethyl isobutyrate → Ethyl 2,2-dimethylpent-4-ynoate

https://huagongshe.com/reaction/751439

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl isobutyrateHCID 7342—
EduktPropargyl bromideHCID 7842—
EduktDiisopropylamineHCID 7912—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexamethylphosphoramideHCID 12679—
ProduktEthyl 2,2-dimethylpent-4-ynoateHCID 14459632—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Diisopropylamine (45.9 mL, 0.33 mol) was dissolved in THF (300 mL) and cooled to 0° C. under N2. n-Butyllithium (131.0 mL, 0.33 mol) was added dropwise over 30 minutes, the mixture was stirred at 0° C. for an additional 30 minutes, and then cooled to −78° C. Ethyl isobutyrate (40 mL, 0.30 mol) was added dropwise in THF (30 mL) and the mixture was stirred at −78° C. for 1 hour. Propargyl bromide (36.4 mL, 0.33 mol) was added dropwise in HMPA (60 mL). The mixture was stirred at −78° C. for 1 hour and then quenched with saturated NH4Cl solution and warmed to room temperature. THF was removed in vacuo, and the residue was dissolved in ether and washed four times with water. The organic layer was dried over MgSO4, filtered, and concentrated. The crude material was distilled under reduced pressure (˜29 inHg, bp 68-70° C.) to obtain the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07405302B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-217e7986ab564cdab624fc66cd10d1b0
Quellennotizuspto-grants-2008_07