TWI555728B - 製備（甲基）丙烯酸酯之方法 - Google Patents
製備（甲基）丙烯酸酯之方法 Download PDFInfo
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- TWI555728B TWI555728B TW097148967A TW97148967A TWI555728B TW I555728 B TWI555728 B TW I555728B TW 097148967 A TW097148967 A TW 097148967A TW 97148967 A TW97148967 A TW 97148967A TW I555728 B TWI555728 B TW I555728B
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- Prior art keywords
- oxygen
- meth
- acrylate
- formula
- reaction
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- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
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- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
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- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
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- 230000001419 dependent effect Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
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- 238000003379 elimination reaction Methods 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 238000002474 experimental method Methods 0.000 description 1
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- IMBKASBLAKCLEM-UHFFFAOYSA-L ferrous ammonium sulfate (anhydrous) Chemical compound [NH4+].[NH4+].[Fe+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O IMBKASBLAKCLEM-UHFFFAOYSA-L 0.000 description 1
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- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
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- 230000000977 initiatory effect Effects 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004998 naphthylethyl group Chemical group C1(=CC=CC2=CC=CC=C12)CC* 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 125000005385 peroxodisulfate group Chemical class 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- PYFQJAMTSYUJMX-UHFFFAOYSA-N phenazine Chemical compound C1=CC=CC2=NC3=CC=CC=C3N=C21.C1=CC=CC2=NC3=CC=CC=C3N=C21 PYFQJAMTSYUJMX-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
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- 239000012966 redox initiator Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
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- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
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- 239000010935 stainless steel Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/12—Esters of monohydric alcohols or phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
- C08F20/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F20/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
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| TW (1) | TWI555728B (enExample) |
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| US9206270B2 (en) * | 2007-12-19 | 2015-12-08 | Evonik Roehm Gmbh | Process for preparing (meth)acrylates |
| US20160090348A1 (en) | 2014-09-30 | 2016-03-31 | Basf Se | Preparation of c8-c24 alkyl (meth)acrylates |
| WO2016071052A1 (de) | 2014-11-05 | 2016-05-12 | Basf Se | Verfahren zur herstellung von c8-c22-alkyl(meth)acrylaten |
| MY185479A (en) * | 2014-12-01 | 2021-05-19 | Basf Se | Process for preparing heonone (meth)acrylate |
| CN107531724B (zh) | 2015-02-26 | 2020-06-23 | 巴斯夫欧洲公司 | 制备异山梨醇乙氧基化物二甲基丙烯酸酯的方法 |
| KR102572781B1 (ko) | 2015-02-26 | 2023-08-31 | 바스프 에스이 | 이소소르비드 디(메트)아크릴레이트의 제조 방법 |
| EP3390338A1 (de) | 2015-12-15 | 2018-10-24 | Basf Se | Verfahren zur herstellung von hydroxybenzophenonpolyglykolether-(meth)acrylat |
| JP7044758B2 (ja) | 2016-08-05 | 2022-03-30 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリイソブテン基を有するマクロモノマー、およびそれらのホモポリマーまたはコポリマー |
| US20240067596A1 (en) * | 2021-01-25 | 2024-02-29 | Basf Se | Continuous method for obtaining 2-ethylhexyl acrylate |
| WO2023143939A1 (de) | 2022-01-26 | 2023-08-03 | Basf Se | Lagerung und/oder transport ethylenisch ungesättigter verbindungen |
| WO2023242259A1 (en) * | 2022-06-15 | 2023-12-21 | Evonik Operations Gmbh | Method for increasing reaction performance by intermediate removal of side product holdup |
| EP4293010A1 (en) * | 2022-06-15 | 2023-12-20 | Evonik Operations GmbH | Process for the discontinuous (trans)esterification of (meth)acrylate compounds |
| EP4299155A1 (en) * | 2022-06-27 | 2024-01-03 | Evonik Operations GmbH | Process to precisely calculate the raw material demand of intermediate batches within a production campaign |
| CN119562975A (zh) * | 2022-10-31 | 2025-03-04 | 三菱化学株式会社 | 含有酯化合物的组合物及其制造方法、聚合性组合物、（甲基）丙烯酸系聚合物及其制造方法 |
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| US20040147772A1 (en) * | 2003-01-17 | 2004-07-29 | Basf Aktiengesellschaft | Preparation of (meth)acrylic esters |
| US20060148928A1 (en) * | 2004-12-30 | 2006-07-06 | Harris William F | Modified latex drag reducer and processes therefor and therewith |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE3423443A1 (de) * | 1984-06-26 | 1986-01-02 | Röhm GmbH, 6100 Darmstadt | Verfahren zur herstellung von estern der acryl- und methacrylsaeure durch umesterung |
| WO1991016037A1 (en) * | 1990-04-16 | 1991-10-31 | Minnesota Mining And Manufacturing Company | Mildness additives for skin cleansing compositions |
| JP3081707B2 (ja) * | 1992-06-16 | 2000-08-28 | ダイセル化学工業株式会社 | メタクリル酸グリシジルの製造方法 |
| JP3513209B2 (ja) * | 1994-03-30 | 2004-03-31 | 積水化学工業株式会社 | 熱可塑性ポリウレタン |
| JPH0931018A (ja) * | 1995-07-24 | 1997-02-04 | Dainippon Ink & Chem Inc | ペンタエリスリトール（メタ）アクリルエステル類の製造法 |
| JPH10175918A (ja) * | 1996-12-18 | 1998-06-30 | Daicel Chem Ind Ltd | （メタ）アクリル酸テトラヒドロベンジルの製造方法 |
| EP0882739A3 (en) | 1997-06-06 | 1999-04-07 | Nippon Shokubai Co., Ltd. | High molecular weight polymer and producing method the same and drag reducer |
| JPH1149810A (ja) | 1997-06-06 | 1999-02-23 | Nippon Shokubai Co Ltd | 高分子量ポリマーおよびその製造方法並びにドラッグレデューサ |
| JPH1180082A (ja) * | 1997-09-10 | 1999-03-23 | Kao Corp | （メタ）アクリル酸高級アルキルエステルの製造法 |
| JP2949150B1 (ja) | 1998-02-27 | 1999-09-13 | 日精化学工業株式会社 | メタクリル酸シクロヘキシルの製造方法 |
| JP2000198835A (ja) * | 1999-01-05 | 2000-07-18 | Daicel Chem Ind Ltd | ヒドロキシアルキル（メタ）アクリラ―ト・メチル置換ε―カプロラクトン変性物含有組成物の製造方法 |
| JP2000319225A (ja) * | 1999-04-28 | 2000-11-21 | Mitsubishi Rayon Co Ltd | メタクリル酸アルキルエステルの製造方法 |
| DE19940622C1 (de) * | 1999-08-27 | 2001-05-17 | Roehm Gmbh | Verfahren zur Herstellung von Di(meth)acrylsäureestern |
| CA2384389A1 (en) * | 2000-08-08 | 2002-02-14 | Kaneka Corporation | Expandable vinyl chloride resin composition |
| EP1201641B1 (en) | 2000-10-23 | 2013-08-14 | Nippon Shokubai Co., Ltd. | Composition of vinyl ether group containing (meth)acrylic acid ester and production method thereof |
| JP2002169220A (ja) * | 2000-11-30 | 2002-06-14 | Mamiya Op Co Ltd | カメラのストラップ用吊金具 |
| JP2004269417A (ja) | 2003-03-07 | 2004-09-30 | Mitsubishi Rayon Co Ltd | （メタ）アクリル酸エステルの製造方法 |
| WO2005040088A1 (ja) | 2003-10-24 | 2005-05-06 | Mitsubishi Rayon Co., Ltd. | (メタ)アクリル酸エステルの製造方法 |
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| JP2006169220A (ja) | 2004-12-20 | 2006-06-29 | Osaka Organic Chem Ind Ltd | （メタ）アクリル酸エステルの製造法 |
| US7361628B2 (en) * | 2004-12-30 | 2008-04-22 | Conocophillips Company | Remote delivery of latex drag-reducing agent without introduction of immiscible low-viscosity flow facilitator |
| TW200728270A (en) * | 2005-11-21 | 2007-08-01 | Toagosei Co Ltd | The manufacture method of (meta) acrylic esters |
| US9206270B2 (en) * | 2007-12-19 | 2015-12-08 | Evonik Roehm Gmbh | Process for preparing (meth)acrylates |
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- 2008-09-29 EP EP08804845.9A patent/EP2220023B1/en active Active
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- 2008-12-17 CN CN200810185589.1A patent/CN101462958B/zh active Active
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| JPH10175919A (ja) * | 1996-12-18 | 1998-06-30 | Daicel Chem Ind Ltd | （メタ）アクリル酸テトラヒドロベンジルの製造法 |
| US20040147772A1 (en) * | 2003-01-17 | 2004-07-29 | Basf Aktiengesellschaft | Preparation of (meth)acrylic esters |
| US20060148928A1 (en) * | 2004-12-30 | 2006-07-06 | Harris William F | Modified latex drag reducer and processes therefor and therewith |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009080380A3 (en) | 2009-09-17 |
| JP2020073555A (ja) | 2020-05-14 |
| JP2014237723A (ja) | 2014-12-18 |
| EP2220023A2 (en) | 2010-08-25 |
| TW200946496A (en) | 2009-11-16 |
| CN101462958B (zh) | 2016-01-20 |
| US9206270B2 (en) | 2015-12-08 |
| EP2220023B1 (en) | 2017-04-05 |
| JP2022081593A (ja) | 2022-05-31 |
| US20100280205A1 (en) | 2010-11-04 |
| WO2009080380A2 (en) | 2009-07-02 |
| US20160046556A1 (en) | 2016-02-18 |
| JP2011506517A (ja) | 2011-03-03 |
| JP2017088608A (ja) | 2017-05-25 |
| CN101462958A (zh) | 2009-06-24 |
| US9688601B2 (en) | 2017-06-27 |
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