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HRID 515147Erstellt: 25. Oktober 2026

(R)-3-Methylmorpholine → HCID 86699725, Verbindung

https://huagongshe.com/reaction/515147

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-3-MethylmorpholineHCID 641498—
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
EduktSodium t-butoxideHCID 23676156—
EduktHCID 86699722HCID 86699722—
Katalysator(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 86699725HCID 8669972522%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

4-Chloro-2-ethylsulfanyl-6-methyl-benzonitrile (synthesized according to the method described in section a) of example 2) (0.20 g, 0.95 mmol), (R)-3-methylmorpholine (0.14 g, 1.42 mmol) and sodium tert-butoxide (0.27 g, 2.85 mmol) are mixed together with dioxane (1 ml) in a microwave vial. The resulting mixture is degassed and flushed with argon for 20 min followed by the addition of (2-biphenyl)di-tert-butylphosphine (0.056 g, 0.19 mmol) and bis(dibenzylideneacetone)-palladium(0) (0.11 g, 0.19 mmol). The reaction mixture is heated at 100° C. in a microwave oven for 1 h. After completion of the reaction (monitored by TLC), the mixture is filtered through a pad of celite and the filtrate is concentrated to get the crude product, which is purified by column chromatography (silica gel, 8% acetone/hexane) to yield 2-ethylsulfanyl-6-methyl-4-[(3R)-3-methyl-morpholin-4-yl]-benzonitrile (0.06 g, 0.217 mmol, 22%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09108936B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-037a5376079b4296b5152f1412deff4b
Quellennotizuspto-grants-2015_08