Production method for isocyanate compound
US-2022002234-A1 · Jan 6, 2022 · US
US12351568B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12351568-B2 |
| Application number | US-201917292249-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 14, 2019 |
| Priority date | Nov 15, 2018 |
| Publication date | Jul 8, 2025 |
| Grant date | Jul 8, 2025 |
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The objective of the present invention is to provide a method for producing a polycarbonate safely and efficiently even without using a base. The method for producing a carbonate derivative according to the present invention is characterized in comprising the step of irradiating a high energy light to a composition comprising the halogenated methane and the hydroxy group-containing compound in the presence of oxygen, wherein a molar ratio of a total usage amount of the hydroxy group-containing compound to 1 mole of the halogenated methane is 0.05 or more.
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The invention claimed is: 1. A method for producing a carbonate derivative, the method consisting of an optional step of stirring a liquid composition comprising a halogenated methane and a hydroxy group-containing compound without irradiating a high energy light, and a step of irradiating the high energy light to the liquid composition in the presence of oxygen to produce the carbonate derivative, and optionally repeating the optional step of stirring and the step of irradiating, wherein the liquid composition does not comprise a base, wherein a molar ratio of a total usage amount of the hydroxy group-containing compound to 1 mole of the halogenated methane is 0.1 or more, wherein the hydroxy group-containing compound is represented by the following formula (i) and the carbonate derivative is a linear carbonate derivative represented by the following formula (I), or the hydroxy group-containing compound is represented by the following formula (ii) and the carbonate derivative is a carbonate derivative comprising a unit represented by the following formula (II-1) or a cyclic carbonate derivative represented by the following formula (II-2): R 1 —OH (i) HO—R 2 —OH (ii) R 1 —O—C(═O)—O—R 1 (I) [—O—R 2 —O—C(═O)—] (II-1) wherein R 1 is a monovalent C 1-200 organic group optionally comprising a hetero atom, R 2 is a divalent C 1-200 organic group optionally comprising a hetero atom. 2. The method according to claim 1 , wherein the halogenated methane is chloroform. 3. The method according to claim 1 , consisting of the step of stirring the composition without irradiating the high energy light. 4. The method according to claim 1 , wherein the high energy light comprises a light having a wavelength of 180 nm or more and 280 nm or less. 5. The method according to claim 1 , wherein two or more kinds of the hydroxy group-containing compound are used.
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