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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 335216Erstellt: 24. Oktober 2026

Diisopropylamine → Methyl 4-bromo-2-methoxy-2-methylpent-4-enoate

https://huagongshe.com/de/reaction/335216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt2,3-DibromopropeneHCID 10552—
EduktPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-bromo-2-methoxy-2-methylpent-4-enoateHCID 86631519109,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A 500 mL round-bottom flask was charged with diisopropylamine (12.89 mL, 92.00 mmol) and dry THF (100 mL) and cooled to −78° C. Butyllithium (2.5 M in hexanes) (36.80 mL, 92.00 mmol) was added dropwise over 20 minutes and the mixture was agitated for additional 30 minutes. Methyl 2-methoxypropanoate (10.35 g, 87.61 mmol) was added dropwise over 20 minutes and the mixture was agitated for 30 minutes. 2,3-Dibromopropene (10.70 mL, 87.61 mmol) was added dropwise over 20 minutes, the mixture was agitated for 30 minutes and then allowed to warm up to ambient temperature and agitated for additional 2 hours. The reaction was quenched with saturated ammonium chloride solution and extracted twice with ether. Extracts were washed with sodium bicarbonate solution, brine, dried and evaporated to give the title compound (22.7 g, 98.4% yield) as pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883828B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-12a6afb9c809476f8edb0aaaa2d93ddc
Quellennotizuspto-grants-2014_11