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HRID 217240Erstellt: 24. Oktober 2026

Dimethyl malonate → Dimethyl cyclopentane-1,1-dicarboxylate

https://huagongshe.com/de/reaction/217240

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl malonateHCID 7943—
Edukt1,4-DibromobutaneHCID 8056—
EduktPotassium CarbonateHCID 11430—
Edukt1-Butyl-3-methylimidazolium tetrafluoroborateHCID 2734178—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktDimethyl cyclopentane-1,1-dicarboxylateHCID 1260960582,3%

Reaktionsschritte

To a solution of malonic acid dimethyl ester (5.28 g, 40 mmol) in DMF (100 ml), 1,4-dibromo-butane (5.26 ml, 44 mmol), K2CO3 (13.8 g, 100 mmol), 1-butyl-3-methylimidazolium tetrafluoroborate (0.904 g, 4.0 mmol) are added at room temperature. The mixture is stirred at room temperature for 15 hours. To the mixture, water is added and the solution is extracted with AcOEt. The organic layer is washed with H2O and brine, dried over MgSO4, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography to give cyclopentane-1,1-dicarboxylic acid dimethyl ester (6.13 g, 82%); TLC (hexane/AcOEt, 5:1) Rf 0.48, 1H NMR (400 MHz, chloroform-d) δ ppm 1.67-1.71 (m, 4H), 2.17-2.21 (m, 4H), 3.72 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193349B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f1910b2b9d6e45aa8fdb51f8d8baf472
Quellennotizuspto-grants-2012_06