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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380469Erstellt: 25. Oktober 2026

Triethylamine → 1-(3,4-Difluorobenzoyl)-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidine

https://huagongshe.com/reaction/380469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3,4-Difluorobenzoyl chlorideHCID 2724519—
Edukt3-(SR)-(4-phenyl piperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidineHCID 20694483—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(3,4-Difluorobenzoyl)-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidineHCID 1836482078,5%

Reaktionsschritte

To a solution of 0.023 g (0.071 mmol) of 3-(SR)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidine and 0.079 mL of Et3N in 2 mL of CH2Cl2 was added 0.059 g (0.28 mmol) of 3,4-difluorobenzoyl chloride and the reaction mixture was stilled for 0.5 h. The reaction mixture was partitioned between CH2Cl2 and sat'd NaHCO3 solution. The organic fraction was dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chomatography (silica, acetone: hexanes, 1:3) to give 0.026 g of the title compound. 1H NMR (CDCl3) δ7.17-7.49 (m, 9H), 7.13 and 7.08 (s, 1H), 7.04 and 6.99 (d, 1H, J=4.6 Hz),4.08-4.15 (m, 2H); Mass Spectrum (CI) m/e=482 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06303593B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-79c3f57b767a4452be5485cb6aa68644
Quellennotizuspto-grants-2001_10