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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 387513Erstellt: 25. Oktober 2026

Diisopropylamine → 4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate

https://huagongshe.com/reaction/387513

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukttert-Butyl bromoacetateHCID 79177—
EduktMethyl 3-(4-chlorophenyl)propanoateHCID 8027172—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinateHCID 6873369681,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

BuLi (5.2 mL, 1.6M in hexanes) was added to a 0° C. solution of diisopropylamine (0.91 g, 9.0 mmol) in THF (40 mL). The reaction mixture was then stirred at 0° C. for 30 minutes, and then cooled to −78° C. A solution of methyl 3-(4-chlorophenyl)propanoate (1.5 g, 7.5 mmol) in THF (8 mL) was added slowly, and the reaction mixture was stirred at −78° C. for 40 minutes. A solution tert-butyl 2-bromoacetate (4.4 g, 22.7 mmol) in THF (5 mL) was then added. The reaction was then stirred for 30 minutes at −78° C. and then warmed to room temperature and stirred overnight. The reaction was then quenched with saturated NH4Cl and concentrated to remove THF. The reaction was then extracted with EtOAc, and the combined extracts were dried (Na2SO4), filtered, concentrated, and dried in vacuo to give 4-tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate (1.91 g, 81%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08372842B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-46182d0ac5b349cb97b46fdf29c5843d
Quellennotizuspto-grants-2013_02