Synthetic intermediate of 1-(2-deoxy-2-fluoro-4-thio-β-D-arabinofuranosyl) cytosine, synthetic intermediate of thionucleoside, and method for producing the same
US-9475835-B2 · Oct 25, 2016 · US
US2016237019A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016237019-A1 |
| Application number | US-201415025379-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 16, 2014 |
| Priority date | Oct 2, 2013 |
| Publication date | Aug 18, 2016 |
| Grant date | — |
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A method for preparing an aromatic carbonate, of the present invention, comprises the steps of: (A) preparing a reaction mixture containing an aliphatic carbonate by reacting an organometallic compound and carbon dioxide; and (B) preparing an aromatic carbonate by reacting the reaction mixture and an aromatic alcohol. The method for preparing an aromatic carbonate allows an aromatic carbonate to be economically prepared in a high yield by using carbon dioxide as a carbonyl supply source.
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1 . A method for preparing an aromatic carbonate, comprising: (A) preparing a reaction mixture containing an aliphatic carbonate by reacting an organometallic compound with carbon dioxide; and (B) preparing an aromatic carbonate by reacting the reaction mixture with an aromatic alcohol. 2 . The method according to claim 1 , wherein the aliphatic carbonate in the reaction mixture is reacted with the aromatic alcohol without being separated. 3 . The method according to claim 1 , wherein the organometallic compound contains a metal-oxygen-carbon bond. 4 . The method according to claim 1 , wherein the organometallic compound comprises at least one of an organometallic compound represented by Formula 1 and an organometallic compound represented by Formula 2: wherein M a is a Group IV or Group XIV element; R 1 is a C 1 to C 12 hydrocarbon group; R 2 is a linear or branched C 1 to C 12 aliphatic hydrocarbon group or a cyclic C 5 to C 12 aliphatic hydrocarbon group; a is an integer from 0 to 2; b is an integer from 2 to 4; and a+b is 4, wherein M b and M c are each independently a Group IV or Group XIV element; R 3 and R 5 are each independently a C 1 to C 12 hydrocarbon group; R 4 and R 6 are each independently a linear or branched C 1 to C 12 aliphatic hydrocarbon group or a cyclic C 5 to C 12 aliphatic hydrocarbon group; c and e are each independently an integer from 0 to 2; d and f are each independently an integer from 1 to 3; and c+d and e+f are each independently 3. 5 . The method according to claim 1 , wherein preparing an aliphatic carbonate (step (A)) is performed at about 130° C. to about 230° C. at a carbon dioxide pressure of about 10 bar to about 200 bar. 6 . The method according to claim 1 , wherein preparing an aromatic carbonate (step (B)) is performed at about 100° C. to about 250° C. at about 1 bar to about 30 bar. 7 . The method according to claim 1 , wherein preparing an aliphatic carbonate (step (A)) is performed in the presence of an alcohol containing a linear or branched C 1 to C 12 aliphatic hydrocarbon group or an alcohol containing a cyclic C 5 to C 12 aliphatic hydrocarbon group.
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