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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873549Erstellt: 24. Oktober 2026

Iodoethane → 5-Cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/de/reaction/1873549

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862547748,1%

Reaktionsschritte

5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a (3.0 g, 14.5 mmol) was dissolved in 60 mL of tetrahydrofuran with stirring followed by addition of ethyl iodide (4.52 g, 29 mmol) and lithium hexamethyldisilazide (29 mL, 29 mmol) under nitrogen atmosphere. The reaction mixture was reacted at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 20 mL of water and extracted with ethyl acetate (200 mL×3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain an oil. TLC showed that there are two adjacent spots, and then the oil was purified by silica gel column chromatography to obtain the title compound 5-cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 19a (1.64 g) as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304411B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-9fdf72cc277e4070a52202139790eb2c
Quellennotizuspto-grants-2012_11