Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895821Generated: October 31, 2026

Dicyclohexylcarbodiimide → 4-(6-Acryloyloxy-hexyloxy)-benzoic acid 4-{2-[4-(6-acryloyloxy-hexyloxy)-phenyl]-ethyl}-phenyl ester

https://huagongshe.com/reaction/1895821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-((6-(Acryloyloxy)hexyl)oxy)benzoic acidHCID 3713565—
ReactantHCID 59386502HCID 59386502—
SolventDichloromethaneHCID 6344—
Product4-(6-Acryloyloxy-hexyloxy)-benzoic acid 4-{2-[4-(6-acryloyloxy-hexyloxy)-phenyl]-ethyl}-phenyl esterHCID 5938649882.4%

Reaction Steps

1.01 g of N,N′-dicyclohexyl carbodiimide was added to a mixture of 1.6 g of 4-{2-[4-(6-acryloyloxy-hexyloxy)-phenyl]-ethyl}-phenol (G), 1.43 g of 4-(6-acryloyloxyhexyloxy)benzoic acid, 0.06 g of 4-N,N-dimethylaminopyridine and 10 ml of dichloromethane stirred in an icebath. After stirring for 2 hours, the ice-bath was removed and the mixture was stirred one night at room temperature. 2.3 g of 4-(6-Acryloyloxy-hexyloxy)-benzoic acid 4-{2-[4-(6-acryloyloxy-hexyloxy)-phenyl]-ethyl}-phenyl ester (10, 78%) was obtained after filtration through silica, evaporation and recrystallizing from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518299B2
Source datasetuspto-grants-2013_08
ORD IDord-c963ca05648746fb93bca9d7a14858b5
Source noteuspto-grants-2013_08