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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1449164Erstellt: 26. Oktober 2026

Nitromethane → 1-p-Fluorobenzyl-2-nitromethylene-pyrrolidine

https://huagongshe.com/reaction/1449164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitromethaneHCID 6375—
EduktDimethyl SulfateHCID 6497—
Edukt2-Pyrrolidinone, 1-((4-fluorophenyl)methyl)-HCID 3045446—
EduktSodiumHCID 5360545—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt1-p-Fluorobenzyl-2-nitromethylene-pyrrolidineHCID 5400911155,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

26.1 g (0.207 mol) of dimethyl sulphate are added to 40 g (0.207 mol) of 1-p-fluorobenzyl-pyrrolidin-2-one and the mixture is heated to 60° for 4 hours. It is then cooled and a solution of sodium methylate prepared from 4.75 g (0.207 gram atom) of sodium and 100 ml of methanol is introduced slowly, at 0°. When the addition is complete, the mixture is stirred for 30 minutes at 50° C. and again cooled to 0°, and 18.9 g (0.31 mol) of nitromethane are added dropwise whilst continuing the stirring. The reaction mixture is left at ambient temperature for 12 hours and is then heated to 50° for 2 hours. It is cooled, and poured into 500 ml of water, which are then extracted with chloroform. The organic layer is now separated off, washed with water and dried over magnesium sulphate, and the solvent is driven off. The residual product is washed with ether and recrystallised from ethanol. 27 g (55.2% yield) of 1-p-fluorobenzyl-2-nitromethylene-pyrrolidine are thus collected in the form of light yellow crystals melting at 108.5°-109°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04189495
Quelldatensatzuspto-grants-1980_02
ORD IDord-c3a6fa5459614821951a4e42b0afd4ef
Quellennotizuspto-grants-1980_02