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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046072Generated: October 25, 2026

2-Bromopropane → HCID 86660609, compound

https://huagongshe.com/reaction/2046072

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 numberUS08592399B2
Source datasetuspto-grants-2013_11
ORD IDord-16997877f6c64bfc8fe6488c3e851a5f
Source noteuspto-grants-2013_11