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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467150Erstellt: 24. Oktober 2026

Triethylamine → 4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetal

https://huagongshe.com/de/reaction/467150

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-(4-Methoxyphenyl)butyric acidHCID 78280—
EduktDiethylphosphorylcyanideHCID 13586794—
EduktBenzene ethyl acetateHCID 21583983—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetalHCID 1513263958%

Reaktionsschritte

L-prolinal dimethyl acetal hydrochloride obtained in the same manner as in Example 1 is dissolved in dimethylformamide (4 ml) containing 4-p-methoxyphenylbutyric acid (740 mg, 3.81 mmol) and diethylphosphoryl cyanide (0.48 ml, 3.16 mmol). To the solution is added dropwise triethylamine (1.15 ml, 8.25 mmol) under cooling and agitation in an ice-methanol bath. After the dropwise addition, the mixture is continued to be stirred for one hour under cooling and then for one hour at room temperature. Benzene-ethyl acetate (2:1, 150 ml) is added to the reaction mixture, and the organic layer is separated, washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml) and a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate and filtered. The filtrate is concentrated to dryness under reduced pressure. The residue is purified by column chromatography on silica gel (benzene-ethyl acetate, 1:2→1:1) to give 727 mg (58%) of the title compound as white crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05158970
Quelldatensatzuspto-grants-1992_10
ORD IDord-be129163bb1b45f48b3bb23d755404ea
Quellennotizuspto-grants-1992_10