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HRID 238943Erstellt: 24. Oktober 2026

Benzyl 2,2,2-trichloroacetimidate → (3S)-3-(benzyloxy)butanoic acid ethyl ester

https://huagongshe.com/de/reaction/238943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl 2,2,2-trichloroacetimidateHCID 144968—
EduktButanoic acid, 3-hydroxy-, ethyl ester, (3S)-HCID 6950306—
KatalysatorTrifluoromethanesulfonic acidHCID 62406—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3S)-3-(benzyloxy)butanoic acid ethyl esterHCID 14201835200,7%

Reaktionsschritte

Under a nitrogen atmosphere, to a solution of (S)-(+)-3-hydroxybutyric acid ethyl ester (100 g, 0.76 mol) in methylene chloride (1.0 L), benzyl 2,2,2-trichloroacetoimidate (381 g, 1.5 mol) and trifluoromethanesulfonic acid (6.7 mL, 76 mmol) were gradually added, and the mixture was stirred at room temperature overnight. The precipitated solid was filtered, and after the mother liquid was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, it was dried with sodium sulfate and the solvent was distilled off under reduced pressure. Hexane was added to the residue, and after the solid was filtered again, the solvent of the mother liquid was distilled off under reduced pressure to give (3S)-3-(benzyloxy)butanoic acid ethyl ester (339 g) as a mixture. The present compound was used for the subsequent reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642640B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-8f6474ba20e846e49214da9fa1a069b8
Quellennotizuspto-grants-2014_02