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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717657Generated: October 25, 2026

2-Bromopropane → HCID 86660609, compound

https://huagongshe.com/reaction/717657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(3-(4-(Diethoxymethyl)phenyl)propyl)-4-fluorobenzenamineHCID 66615110—
Reactant4-(3-(4-Fluorophenylamino)propyl)benzaldehydeHCID 86660610—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 86660609HCID 8666060983%

Reaction Steps

A mixture of 4-(3-(4-fluorophenylamino)propyl)benzaldehyde (0.09 g, 0.35 mmol) [prepared form the product of Step B by stirring in acidifies CHCl3] and 2-bromopropane (0.2 ml) and K2CO3 (0.1 g; 0.73 mmol) was stirred at reflux in anhydrous DMF (5 ml) for 6 h. The solvent was evaporated under reduced pressure and the residue was diluted to 50 ml with EtOAc and washed with H2O. The organic layer separated and dried over MgSO4 and filtered. The filtrate was evaporated to dryness and the residue was purified by FCC(SiO2, hexane/EtOAc), to give the title compound (0.078 g, 83%) as creamy paste. 1H-NMR (CDCl3) 10 (s, 1H); 7.78 (d, 2H, J=8.13 Hz); 7.32 (d, 2H, J=8.07 Hz); 6.93-6.86 (m, 2H); 6.82-6.66 (m, 2H); 3.07 (t, 2H, J=7.5 Hz); 2.71 (t, 2H, J=7.5 Hz); 2.71 (t, 2H, 7.62 Hz); 2.27-2.21 (m, 1H); 1.86-1.83 (m, 1H); 1.08 (d, 6H, J=6.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193716B2
Source datasetuspto-grants-2015_11
ORD IDord-a2f0025702d649f8b1148e3b58c23a92
Source noteuspto-grants-2015_11