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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384971Erstellt: 24. Oktober 2026

Water → HCID 66610575, Verbindung

https://huagongshe.com/de/reaction/384971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt(R)-dimethyl 2-(3-(2,3-dihydro-1H-inden-1-ylamino)allylidene)malonateHCID 86649726—
LösungsmittelMethanolHCID 887—
ProduktHCID 66610575HCID 6661057593,4%

Reaktionsschritte

To a solution of 11.0 g (1.0 eq) (R)-dimethyl 2-(3-(2,3-dihydro-1H-inden-1-ylamino)allylidene)malonate in 80 ml dry MeOH was slowly added 3.65 g (2.5 eq) NaH (60% dispersion in mineral oil) under N2 protection. The reaction was stirred at room temperature for 10 minutes and was then heated at 60° C. After 20 minutes, to the reaction mixture were added 30 ml water. The resulting mixture was heated at 60° C. for an additional 20 minutes. The solvent was removed in vacuo. The residue was diluted with 50 ml water, and extracted with hexane (2×50 ml) to remove mineral oil. Then the aqueous mixture was acidified with 2N HCl to pH 1-2 and extracted with ethyl acetate (2×100 ml). The combined organic phase was washed with 100 ml brine, dried over sodium sulfate and concentrated in vacuo to afford (R)-1-(2,3-dihydro-1H-inden-1-yl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid as a white solid (8.7 g, yield 93%) which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367836B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-543b552766514cec86e03f43336154ea
Quellennotizuspto-grants-2013_02