HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 14692538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4'-(Octyloxy)-[1,1'-biphenyl]-4-carboxylic acid | HCID 2802556 | — |
| Reactant | (S)-1-(3-Pyridyl)ethanol | HCID 10725338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14692538 | HCID 14692538 | 7.1% |
Reaction Steps
(S)-1-(3-pyridyl)ethanol (2.0 g) prepared in the above item (ii), 4-octyloxybiphenyl-4'-carboxylic acid (5.3 g), dicyclohexylcarbodiimide (5.7 g) and dimethylaminopyridine (0.2 g) were dissolved in methylene chloride (100 ml), followed by agitating the solution for 15 hours, thereafter filtering off insolubles, washing the filtrate with water, concentrating it and recrystallizing from a mixed solvent of heptane-toluene to obtain (S)-4-octyloxybiphenyl-4'-carboxylic acid-1-(3-pyridyl)ethyl ester (0.5 g). M.P.: 77.5-78.5° C. Specific angle of rotation [a]D25 =+95° (c=1.0, CHCl3). Further, the structure of this product was confirmed according to NMR spectra and the product accorded with the captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04965018 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-1404b9a84baa494c8d85e9e7b695d557 |
| Source note | uspto-grants-1990_10 |