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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180177Generated: October 26, 2026

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

https://huagongshe.com/reaction/2180177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Iodo-phenyl)-4-(isobutoxycarbonylamino-methyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 68533882—
SolventDichloromethaneHCID 6344—
Product[4-(4-Iodo-phenyl)-piperidin-4-ylmethyl]-carbamic acid isobutyl esterHCID 6853426693.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887889B2
Source datasetuspto-grants-2005_05
ORD IDord-4780461f77634f3ca7b20458ac6fa570
Source noteuspto-grants-2005_05