JP2003064113A5 - - Google Patents
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- JP2003064113A5 JP2003064113A5 JP2001252853A JP2001252853A JP2003064113A5 JP 2003064113 A5 JP2003064113 A5 JP 2003064113A5 JP 2001252853 A JP2001252853 A JP 2001252853A JP 2001252853 A JP2001252853 A JP 2001252853A JP 2003064113 A5 JP2003064113 A5 JP 2003064113A5
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- organic peroxide
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- 0 CC(C)(*)OOC(C)(*)OOC(*)(CN)C=* Chemical compound CC(C)(*)OOC(C)(*)OOC(*)(CN)C=* 0.000 description 1
Description
【特許請求の範囲】
【請求項1】
双極子モーメント0.5以下で、沸点若しくは初留温度が110℃以上の溶媒10〜50%及び該溶媒に溶解した下記式(1)
(式中、R 1 は炭素数2から20のアルキル基、または水酸基で置換された炭素数1から20のアルキル基、アルコキシ基で置換された炭素数1から20のアルキル基、R 2 、R 3 はそれぞれ、炭素数2から20のアルキル基、または水酸基で置換された炭素数2から20のアルキル基、アルコキシ基で置換された炭素数2から20のアルキル基、フェニル基、またはアルキル基で置換されたフェニル基、シクロアルキル基、またはアルキル基で置換されたシクロアルキル基を表す)
で示される有機過酸化物50%〜90%を含む有機過酸化物組成物。
【請求項2】
溶媒が初留温度140℃以上のイソパラフィン溶媒である請求項1に記載の有機過酸化物組成物。
【請求項3】
下記式(1’)で示される新規有機過酸化物
(式中、R1’は、置換基として水酸基又はアルコキシ基を有する炭素数1から20のアルキル基、R2、R3はそれぞれ、炭素数2から20のアルキル基、または水酸基で置換された炭素数2から20のアルキル基、アルコキシ基で置換された炭素数2から20のアルキル基、フェニル基、またはアルキル基で置換されたフェニル基、シクロアルキル基、またはアルキル基で置換されたシクロアルキル基を表す)
【請求項4】
請求項1に記載の有機過酸化物組成物を使用することを特徴とするアクリル樹脂の製造方法。
【請求項5】
式(1)におけるR1が水酸基又はアルコキシ基で置換された炭素数1から20のアルキル基である請求項4に記載のアクリル樹脂の製造方法。
【請求項6】
式(1)におけるR2及びR3がそれぞれ、水酸基で置換された炭素数2から20のアルキル基又はアルコキシ基で置換された炭素数2から20のアルキル基である請求項4または5に記載のアクリル樹脂の製造方法。
【請求項7】
請求項2に記載の有機過酸化物組成物を使用することを特徴とするアクリル樹脂の製造方法。
[Claims]
[Claim 1 ]
10-50% of a solvent having a dipole moment of 0.5 or less and a boiling point or initial boiling temperature of 110 ° C. or more, and the following formula (1) dissolved in the solvent:
(Wherein, R 1 is an alkyl group having 2 to 20 carbon atoms, an alkyl group having 1 to 20 carbon atoms substituted with a hydroxyl group, an alkyl group having 1 to 20 carbon atoms substituted with an alkoxy group, R 2 , R 2 3 is an alkyl group having 2 to 20 carbon atoms, an alkyl group having 2 to 20 carbon atoms substituted with a hydroxyl group, an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group, a phenyl group, or an alkyl group, respectively. Represents a substituted phenyl group, a cycloalkyl group, or a cycloalkyl group substituted with an alkyl group)
An organic peroxide composition containing 50% to 90% of an organic peroxide represented by the formula:
[Claim 2 ]
The organic peroxide composition according to claim 1 , wherein the solvent is an isoparaffin solvent having an initial distillation temperature of 140 ° C or higher.
[Claim 3 ]
Novel organic peroxide represented by the following formula (1 ′)
(Wherein, R 1 ′ is an alkyl group having 1 to 20 carbon atoms having a hydroxyl group or an alkoxy group as a substituent, and R 2 and R 3 are each substituted with an alkyl group having 2 to 20 carbon atoms or a hydroxyl group. An alkyl group having 2 to 20 carbon atoms, an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group, a phenyl group, or a phenyl group substituted with an alkyl group, a cycloalkyl group, or a cycloalkyl substituted with an alkyl group; Represents a group)
[Claim 4 ]
Method of manufacturing features and to luer acrylic resin using an organic peroxide composition according to claim 1.
[Claim 5 ]
The method for producing an acrylic resin according to claim 4 , wherein R1 in the formula (1) is an alkyl group having 1 to 20 carbon atoms and substituted with a hydroxyl group or an alkoxy group.
[ 6 ]
The acrylic according to claim 4 or 5 , wherein R2 and R3 in the formula (1) are each an alkyl group having 2 to 20 carbon atoms substituted with a hydroxyl group or an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group. Method of manufacturing resin.
7.
A method for producing an acrylic resin, comprising using the organic peroxide composition according to claim 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001252853A JP4774172B2 (en) | 2001-08-23 | 2001-08-23 | Acrylic resin production method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001252853A JP4774172B2 (en) | 2001-08-23 | 2001-08-23 | Acrylic resin production method |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2003064113A JP2003064113A (en) | 2003-03-05 |
JP2003064113A5 true JP2003064113A5 (en) | 2008-10-02 |
JP4774172B2 JP4774172B2 (en) | 2011-09-14 |
Family
ID=19081258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001252853A Expired - Lifetime JP4774172B2 (en) | 2001-08-23 | 2001-08-23 | Acrylic resin production method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4774172B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2971510B1 (en) * | 2011-02-10 | 2013-03-22 | Arkema France | RADICAL POLYMERIZATION OF ETHYLENE STARCHED WITH HIGH-PRODUCTIVITY ORGANIC PEROXIDES |
JP5861824B2 (en) * | 2011-11-17 | 2016-02-16 | スリーボンドファインケミカル株式会社 | Thermosetting composition |
WO2013146048A1 (en) * | 2012-03-27 | 2013-10-03 | 日本ゼオン株式会社 | Method for producing toner |
FR3041645B1 (en) * | 2015-09-29 | 2017-09-08 | Arkema France | RADICAL POLYMERIZATION OF ETHYLENE PRIMERED BY A COUPLE OF HIGH-PRODUCTIVITY ORGANIC PEROXIDES |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5791250A (en) * | 1980-11-28 | 1982-06-07 | Shin Etsu Chem Co Ltd | Preparation of conductive silicone rubber sponge |
JPS63168415A (en) * | 1987-01-02 | 1988-07-12 | ペンウオルト・コ−ポレ−シヨン | Solution polymerization of acrylic acid derivative monomer using t-alkylhydroxyperoxide |
-
2001
- 2001-08-23 JP JP2001252853A patent/JP4774172B2/en not_active Expired - Lifetime
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