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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246021Generated: October 31, 2026

Potassium Carbonate → bis[6-{4-[(1E)-3-(4-pentyloxyphenoxy)-3-oxoprop-1-enyl]phenoxy}hexyl]2,2 bis(4-nitrobenzyl)malonate

https://huagongshe.com/reaction/2246021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBis[6-chlorohexyl]2,2 bis(4-nitrobenzyl)malonateHCID 59217445—
Reactant4-pentoxyphenyl (2E)-3-{4-hydroxyphenyl}acrylateHCID 59217449—
CatalystTetrabutylammonium IodideHCID 67553—
SolventMethyl Ethyl KetoneHCID 6569—
Productbis[6-{4-[(1E)-3-(4-pentyloxyphenoxy)-3-oxoprop-1-enyl]phenoxy}hexyl]2,2 bis(4-nitrobenzyl)malonateHCID 5921745265.7%

Reaction Steps

2.80 g (4.6 mmol) bis[6-chlorohexyl]2,2 bis(4-nitrobenzyl)malonate, 3.0 g (9.2 mmol) 4-pentoxyphenyl (2E)-3-{4-hydroxyphenyl}acrylate and 0.17 g (0.46 mmol) tetrabutylammonium iodide were dissolved in 30 ml 2-butanone. 2.53 g (18.3 mmol) potassium carbonate were added. The resulting suspension was heated at refluxing temperature and allowed to react for 48 h. After cooling to room temperature, the reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed repeatedly with water, dried over sodium sulfate, filtered and concentrated by rotary evaporation to yield 3.6 g bis[6-{4-[(1E)-3-(4-pentyloxyphenoxy)-3-oxoprop-1-enyl]phenoxy}hexyl]2,2 bis(4-nitrobenzyl)malonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687118B2
Source datasetuspto-grants-2010_03
ORD IDord-ce48a12435f341ad8e83dfeb50492dd5
Source noteuspto-grants-2010_03