HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → Cyclohexane-1,4-dicarboxylic acid 1-[4-(11-acryloyloxy-undecyl)phenyl]ester 4-(4-hexylphenyl)ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Hexylphenol | HCID 18594 | — |
| Reactant | 4-(11-Acryloyloxyundecyl)phenol | HCID 59386490 | — |
| Reactant | HCID 178525731 | HCID 178525731 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Cyclohexane-1,4-dicarboxylic acid 1-[4-(11-acryloyloxy-undecyl)phenyl]ester 4-(4-hexylphenyl)ester | HCID 59386492 | 25% |
Reaction Steps
2.5 g of N,N′-dicyclohexyl carbodiimide was added to a mixture of 2.0 g of 4-(11-acryloyloxyundecyl)phenol (G), 1.1 g of hexylphenol (E), 1.03 g of trans-cyclohexane-1,4-dicarboxylic acid (F), 0.15 g of 4-N,N-dimethylaminopyridine and 50 ml of dichloromethane, cooled in an ice bath and stirred under a nitrogen atmosphere. The mixture was stirred overnight at room temperature. 0.93 g of cyclohexane-1,4-dicarboxylic acid 1-[4-(11-acryloyloxy-undecyl)phenyl]ester 4-(4-hexylphenyl)ester (6, 25%) was obtained as a white powder after evaporation, and separation by chromatography using silica gel and dichloromethane/petroleum ether 97/3 as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763330B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-fd8d8dec088b4a7398f6eb374101182e |
| Source note | uspto-grants-2010_07 |