Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262590Generated: November 2, 2026

HCID 21319307, compound → HCID 21319303, compound

https://huagongshe.com/reaction/262590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21319307HCID 21319307—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 21319303HCID 2131930380.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154850
Source datasetuspto-grants-1979_05
ORD IDord-39b2cc1b50154b299fa36eda4c368a5a
Source noteuspto-grants-1979_05