HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21319307, compound → HCID 21319303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21319307 | HCID 21319307 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21319303 | HCID 21319303 | 80.3% |
Reaction Steps
1-(4-ethoxycarbonylphenoxy)-14-(4-chlorophenoxy)-tetradec 9-yne (2.00 g.; 0.0041 M.) in acetic acid (15 ml.) was reduced in the presence of hydrogen and PtO2 (0.05 g.) at 60° C. and atmospheric pressure. When hydrogen absorption was complete the solution was filtered, the catalyst washed well with ethanol and the solvents evaporated under reduced pressure to yield a colourless oil. 1-(4-ethoxycarbonylphenoxy)-14-(4-chlorophenoxy)-tetradecane (1.62 g.; 80%) M.P. 72.5°-73.5° C. was obtained as a pure crystalline compound by chromatography of this oil on silica-gel (100 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04154850 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-39b2cc1b50154b299fa36eda4c368a5a |
| Source note | uspto-grants-1979_05 |