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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467151Erstellt: 23. Oktober 2026

Triethylamine → HCID 15132640, Verbindung

https://huagongshe.com/de/reaction/467151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt(2R)-1-[(tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 688022—
EduktDiethylphosphorylcyanideHCID 13586794—
EduktBenzene ethyl acetateHCID 21583983—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 15132640HCID 1513264063%

Reaktionsschritte

L-prolinal dimethyl acetal hydrochloride obtained in the same manner as in Example 1 is dissolved in dimethylformamide (4 ml) containing tert-butoxycarbonyl-D-proline (790 mg, 3.17 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. 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 713 mg (63%) of the title compound as a pale yellow syrup.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05158970
Quelldatensatzuspto-grants-1992_10
ORD IDord-fa19b9577d11491c9393047d151120d8
Quellennotizuspto-grants-1992_10