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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494123Erstellt: 25. Oktober 2026

Iodine → (S)-1-Ethyl-5-methylpiperazin-2-one

https://huagongshe.com/reaction/494123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTolueneHCID 1140—
EduktDicyclohexyl(ethyl)phosphineHCID 17909966—
Edukt1-ethyl-5-methylpyrazin-2(1H)-oneHCID 68865636—
KatalysatorHCID 178478077HCID 178478077—
LösungsmittelMethanolHCID 887—
Produkt(S)-1-Ethyl-5-methylpiperazin-2-oneHCID 44630611—

Reaktionsschritte

A mixture of chloro-1,5-cyclooctadiene iridium (I) dimer (34 mg, 51 μmol) and (S)-1-[(R)-2-di-(3,5-bis(trifluoromethyl)phenyl)phosphino)ferrocenyl]ethyldicyclohexylphosphine (44 mg, 51 μmol; Solvias AG, SL-J006-2) in a mixture of 1:2 toluene and methanol (100 mL; purged with nitrogen for 15 minutes) was sonicated under an atmosphere of nitrogen for 15 minutes. To the resultant mixture, iodine (0.39 g, 1.52 mmol) and 1-ethyl-5-methylpyrazin-2(1H)-one (7.0 g, 50.66 mmol) was added. The resultant mixture was heated in an oil bath at 50° C. under an atmosphere of hydrogen gas at 800 psi for 48 hours. The product mixture was filtered through a pad of Celite. The filtrate was concentrated under vacuum. The residue was treated with chloroform saturated with ammonia gas (100 mL). The resultant suspension was filtered through a pad of Celite, which was the rinsed with chloroform saturated with ammonia gas. The combined filtrate was concentrated under vacuum. The residue was concentrated as a solution in toluene for subsequent reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538112B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-e899bbb6069b4e1aaf4ca6aae333dea1
Quellennotizuspto-grants-2009_05