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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2180177Erstellt: 24. Oktober 2026

Trifluoroacetic acid → [4-(4-Iodo-phenyl)-piperidin-4-ylmethyl]-carbamic acid isobutyl ester

https://huagongshe.com/de/reaction/2180177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt4-(4-Iodo-phenyl)-4-(isobutoxycarbonylamino-methyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 68533882—
LösungsmittelDichloromethaneHCID 6344—
Produkt[4-(4-Iodo-phenyl)-piperidin-4-ylmethyl]-carbamic acid isobutyl esterHCID 6853426693,3%

Reaktionsschritte

To a stirred solution of 4-(4-iodo-phenyl)-4-(isobutoxycarbonylamino-methyl)-piperidine-1-carboxylic acid tert-butyl ester (0.075 g, 0.15 mmol) in CH2Cl2 (1.5 mL) at 0° C. was added TFA (0.5 mL). The mixture was stirred at room temperature for 3 h. TLC (4:1 hexanes/EtOAc) showed no starting material left. The solvent was removed by rotary evaporation and the resulting liquid was evaporated from toluene (2×10 mL), diluted with EtOAc (100 mL) and washed with 10% aqueous NaHCO3 solution (2×50 mL) and saturated brine (50 mL). The organic layer was dried over anhydrous Na2SO4, filtered, concentrated by rotary evaporation and dried under high vacuum for 1 h to give [4-(4-iodo-phenyl)-piperidin-4-ylmethyl]-carbamic acid isobutyl ester as a reddish solid (0.058 g, ˜0.14 mmol). MS (ESI): 417.1/418.1(M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06887889B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-4780461f77634f3ca7b20458ac6fa570
Quellennotizuspto-grants-2005_05