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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1917330Erstellt: 26. Oktober 2026

Trifluoroacetic acid → rel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylate

https://huagongshe.com/reaction/1917330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
EduktMethyl cyclopent-1-ene-1-carboxylateHCID 549129—
LösungsmittelDichloromethaneHCID 6344—
Produktrel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylateHCID 151551483%

Reaktionsschritte

A catalytic amount of trifluoroacetic acid was added to a solution of 1-cyclopentene-1-carboxylic acid methyl ester (2.52 g, 20.0 mmol) and N-benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine (5.00 g, 21.1 mmol) in dichloromethane (40 mL) at room temperature, and the mixture was heated with stirring at room temperature for 15.5 hours. The reaction solution was diluted with dichloromethane (100 mL) and washed with a saturated sodium bicarbonate solution (80 mL). The washed aqueous layer was further extracted with dichloromethane (50 mL). The organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5→90:10→80:20) to give 4.28 g (83%) of the title compound as a colorless transparent oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618094B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-0be8207185c648c4ab86050b9ee72355
Quellennotizuspto-grants-2013_12