HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 19103571, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 2-Fluoro-4-hydroxybenzonitrile | HCID 2734675 | — |
| Reactant | 4-butoxy-2-fluorobenzoic acid | HCID 2773434 | — |
| Reactant | 2,3-Difluoro-4-octylphenol | HCID 14495630 | — |
| Reactant | HCID 86747516 | HCID 86747516 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19103571 | HCID 19103571 | — |
Reaction Steps
0.1 mol of 2-fluoro-4-butyloxybenzoic acid (prepared from 3-fluoro-4-cyanophenol by alkylation with butyl bromide/potassium carbonate in dimethylformamide and subsequent hydrolysis of the nitrile via the imido ester), 0.01 mol of dimethylaminopyridine and 0.1 mol of 2,3-difluoro-4-octylphenol are initially introduced into 150 ml of methylene chloride, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of methylene chloride is added dropwise at 10°, while stirring, and the mixture is then subsequently stirred at room temperature for 15 hours. The mixture is filtered over silica gel and the solvent is evaporated to give 2,3-difluoro-4-octylphenyl 2-fluoro-4-butyloxybenzoate as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05279764 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-72f8c0cb865949ab9d7c8822f601ff6b |
| Source note | uspto-grants-1994_01 |