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HRID 415977Erstellt: 24. Oktober 2026

Ammonium Chloride → 1-Cyclohexyl-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one

https://huagongshe.com/de/reaction/415977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktN-Cyclohexyl-2-pyrrolidoneHCID 81278—
EduktLithium diisopropylamideHCID 2724682—
Edukt2-(Bromomethyl)-1,3-dichloro-5-methoxybenzeneHCID 59299479—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Cyclohexyl-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-oneHCID 5929941469%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Dissolve commercially available 1-cyclohexyl-pyrrolidin-2-one (88.2 g, 527.9 mmol) in 2500 mL tetrahydrofuran and cool to −78° C. Add 176 mL 2 M LDA and stir for ˜5 min. Add 2-bromomethyl-1,3-dichloro-5-methoxy-benzene (95 g, 351.9 mmol) and allow the reaction to warm to room temperature. Pour the mixture into saturated ammonium chloride and extract twice with dichloromethane. Dry over sodium sulfate, filter and concentrate under vacuum to obtain a tan solid. Add hexanes and stir rapidly before filtering. Wash the filter cake several times with cold hexane to obtain 86 g (69%) of a light-tan solid: MS (m/z): 356 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088776B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-671ed090c526489ea143d527e9a47bc2
Quellennotizuspto-grants-2012_01