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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2198778Erstellt: 24. Oktober 2026

Sodium Chloride → Methyl 2,2,5-trimethyl-4-hexenoate

https://huagongshe.com/de/reaction/2198778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktMethyl isobutyrateHCID 11039—
Edukt2-Butene, 1-bromo-3-methyl-HCID 70092—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktMethyl 2,2,5-trimethyl-4-hexenoateHCID 550269—

Reaktionsschritte

300 g. of a 10% solution of lithium diisopropylamide in hexane was introduced into 90 ml. of absolute tetrahydrofuran, cooled to 0°, and combined dropwise under agitation with a solution of 28 g. of isobutyric acid methyl ester in 150 ml. of absolute tetrahydrofuran. The reaction solution was stirred for one hour at 0°, then cooled to -40° and subsequently added to a solution of 58 g. of 4-bromo-2-methyl-2-butene (dimethylallyl bromide) in 60 ml. of absolute dimethyl sulfoxide, maintained at -20°. While allowing the temperature of the solution to rise to room temperature, the solution was stirred for 6 hours and then combined with saturated sodium chloride solution. The organic phase was separated, the aqueous phase was extracted five times with respectively 200 ml. of a 1/1 mixture of ether and hexane. The combined organic phases were washed neutral with 0.5 N hydrochloric acid and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated on a forced circulation evaporator. The residue was distilled under vacuum, thus obtaining 20.7 g. of the title compound, b.p. (13 mm.) 74°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04359467
Quelldatensatzuspto-grants-1982_11
ORD IDord-047418f600a44e3cb4e3cdbc8afef10e
Quellennotizuspto-grants-1982_11