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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22288Erstellt: 24. Oktober 2026

Acetic Anhydride → HCID 54082237, Verbindung

https://huagongshe.com/de/reaction/22288

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt1-Benzylpiperidine-4-carbaldehydeHCID 89584—
EduktLithium diisopropylamideHCID 2724682—
Edukt3,4-Dihydrocyclopenta(b)indol-1(2H)-oneHCID 6424669—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 54082237HCID 54082237—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a mixture of 1,2,3,4-tetrahydrocyclopent[b]-indol-1-one (440 mg, 2.6 mmol) and 1-benzylpiperidine-4-carboxaldehyde (581 mg, 2.86 mmol) in 90 ml dry THF was added 5.4 mmol of lithium diisopropylamide at -78° C. The mixture was stirred at -78° C. for 30 minutes, then warmed up to 0° C. for 1.5 hours, and then to r.t. for 15 minutes. Acetic anhydride (0.265 g, 2.6 mmol) was added, the mixture was stirred at r.t. for 1.5 hours and quenched ammonium chloride, water and extracted with chloroform. The organic layer was dried, concentrated, and purified through silica gel to give the title compound. 1HNMR (CDCl3)δ 1.45-1.7 (m, 3H), 1.8-2.3 (m, 4H), 2.8-3.0 (m, 2H), 3.46 (s, 2H), 3.55 (s, 2H), 6.5 (m, 1H), 7.1-7.4 (m, 8H), 7.9 (m, 1H), 9.2 (s, 1H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428043
Quelldatensatzuspto-grants-1995_06
ORD IDord-38dbbafc6f744e7f8c4c06aaaa9e7d7c
Quellennotizuspto-grants-1995_06