JP4773441B2 - 3−(メチルチオ)プロパナールの製造方法 - Google Patents
3−(メチルチオ)プロパナールの製造方法 Download PDFInfo
- Publication number
- JP4773441B2 JP4773441B2 JP2007524209A JP2007524209A JP4773441B2 JP 4773441 B2 JP4773441 B2 JP 4773441B2 JP 2007524209 A JP2007524209 A JP 2007524209A JP 2007524209 A JP2007524209 A JP 2007524209A JP 4773441 B2 JP4773441 B2 JP 4773441B2
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- acrolein
- process according
- mmp
- reaction
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- CLUWOWRTHNNBBU-UHFFFAOYSA-N 3-methylthiopropanal Chemical compound CSCCC=O CLUWOWRTHNNBBU-UHFFFAOYSA-N 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims description 86
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 65
- 239000003054 catalyst Substances 0.000 claims description 63
- 238000000034 method Methods 0.000 claims description 30
- 239000012429 reaction media Substances 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011347 resin Substances 0.000 claims description 18
- 239000004793 Polystyrene Substances 0.000 claims description 11
- 229920002223 polystyrene Polymers 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 8
- VWWOJJANXYSACS-UHFFFAOYSA-N 2-hydroxy-4-methylsulfanylbutanenitrile Chemical compound CSCCC(O)C#N VWWOJJANXYSACS-UHFFFAOYSA-N 0.000 claims description 5
- 239000002638 heterogeneous catalyst Substances 0.000 claims description 4
- 125000006264 diethylaminomethyl group Chemical group [H]C([H])([H])C([H])([H])N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims description 3
- -1 dimethylaminoethyl Chemical group 0.000 claims description 3
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 239000000025 natural resin Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 239000000057 synthetic resin Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 62
- 102000002274 Matrix Metalloproteinases Human genes 0.000 description 48
- 108010000684 Matrix Metalloproteinases Proteins 0.000 description 48
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 19
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 238000010924 continuous production Methods 0.000 description 9
- 239000006227 byproduct Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000004821 distillation Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000007790 solid phase Substances 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical compound OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 4
- 229930182817 methionine Natural products 0.000 description 4
- 229960004452 methionine Drugs 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010923 batch production Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HBAHZZVIEFRTEY-UHFFFAOYSA-N 2-heptylcyclohex-2-en-1-one Chemical compound CCCCCCCC1=CCCCC1=O HBAHZZVIEFRTEY-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- 0 C*(*)CCN(*)* Chemical compound C*(*)CCN(*)* 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 229920001367 Merrifield resin Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- JUUZQMUWOVDZSD-UHFFFAOYSA-N 1h-imidazole;pyrazine Chemical compound C1=CNC=N1.C1=CN=CC=N1 JUUZQMUWOVDZSD-UHFFFAOYSA-N 0.000 description 1
- MTAODLNXWYIKSO-UHFFFAOYSA-N 2-fluoropyridine Chemical compound FC1=CC=CC=N1 MTAODLNXWYIKSO-UHFFFAOYSA-N 0.000 description 1
- QJDRJTFSPVQEDV-UHFFFAOYSA-N 2-methylbutanethioic s-acid Chemical compound CCC(C)C(O)=S QJDRJTFSPVQEDV-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 206010019332 Heat exhaustion Diseases 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-ZQBYOMGUSA-N [14c]-nicotinamide Chemical compound N[14C](=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-ZQBYOMGUSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 150000001913 cyanates Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- MUQBUKGCVPYANP-UHFFFAOYSA-N formonitrile Chemical compound N#C.N#C MUQBUKGCVPYANP-UHFFFAOYSA-N 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- FFEARJCKVFRZRR-UHFFFAOYSA-N methionine Chemical compound CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
- C07C319/20—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
- C07C319/18—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by addition of thiols to unsaturated compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004038053.8 | 2004-08-05 | ||
| DE102004038053A DE102004038053A1 (de) | 2004-08-05 | 2004-08-05 | Verfahren zur Herstellung von 3-(Methylthio)propanal |
| PCT/EP2005/007666 WO2006015684A2 (de) | 2004-08-05 | 2005-07-14 | Verfahren zur herstellung von 3-(methylthio)propanal und 2-hydroxy-4-(methylthio)butannitril |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011066503A Division JP5306402B2 (ja) | 2004-08-05 | 2011-03-24 | 3−(メチルチオ)プロパナールの製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008508330A JP2008508330A (ja) | 2008-03-21 |
| JP2008508330A5 JP2008508330A5 (enExample) | 2011-05-12 |
| JP4773441B2 true JP4773441B2 (ja) | 2011-09-14 |
Family
ID=35149290
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007524209A Expired - Fee Related JP4773441B2 (ja) | 2004-08-05 | 2005-07-14 | 3−(メチルチオ)プロパナールの製造方法 |
| JP2011066503A Expired - Fee Related JP5306402B2 (ja) | 2004-08-05 | 2011-03-24 | 3−(メチルチオ)プロパナールの製造方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011066503A Expired - Fee Related JP5306402B2 (ja) | 2004-08-05 | 2011-03-24 | 3−(メチルチオ)プロパナールの製造方法 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7119233B2 (enExample) |
| EP (2) | EP2987785B1 (enExample) |
| JP (2) | JP4773441B2 (enExample) |
| CN (2) | CN101031542B (enExample) |
| BR (1) | BRPI0513072A (enExample) |
| CA (1) | CA2573047A1 (enExample) |
| DE (1) | DE102004038053A1 (enExample) |
| ES (2) | ES2667220T3 (enExample) |
| MX (1) | MX2007000345A (enExample) |
| RU (1) | RU2383531C2 (enExample) |
| WO (1) | WO2006015684A2 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005003990A1 (de) * | 2005-01-28 | 2006-08-03 | Degussa Ag | Herstellung von 3-(Alkylthio)propanal |
| JP5182198B2 (ja) * | 2009-04-06 | 2013-04-10 | 住友化学株式会社 | 3−メチルチオプロパナールの製造方法 |
| JP5402864B2 (ja) * | 2010-07-20 | 2014-01-29 | 住友化学株式会社 | 3−メチルチオプロパナールの製造方法 |
| FR2966456B1 (fr) * | 2010-10-26 | 2013-03-15 | Adisseo France Sas | Procede d'obtention d'acroleine par deshydratation catalytique de glycerol ou de glycerine |
| EP2468383A1 (de) * | 2010-12-22 | 2012-06-27 | Evonik Degussa GmbH | Verfahren zur thermischen Nachverbrennung von Abgasen aus der Acrolein- und aus der Blausäureherstellung |
| MY161682A (en) * | 2011-02-23 | 2017-05-15 | Evonik Degussa Gmbh | Storage-stable 2-hydroxy-4- (methylthio) butyronitrile |
| BR112013018092B1 (pt) | 2011-02-23 | 2021-04-27 | Evonik Operations Gmbh | Método para produção de 2-hidróxi-4-(metiltio) butano nitrila a partir de 3- (metiltio) propanal e cianeto de hidrogênio, e uso de um produto de reação, que contém mmp-cianidrina |
| EP3004041B1 (de) | 2013-06-03 | 2020-05-06 | Evonik Operations GmbH | Verfahren zur herstellung von acrolein |
| CN107417570B (zh) * | 2017-09-14 | 2020-04-14 | 哈尔滨理工大学 | 利用丙酮氰醇制备α-羟基腈的方法 |
| CN111116437B (zh) | 2018-11-01 | 2021-02-05 | 山东新和成氨基酸有限公司 | 制备2-羟基-4-甲硫基丁酸及其中间体的方法和装置 |
| CN109651215B (zh) * | 2019-02-14 | 2023-12-22 | 天宝动物营养科技股份有限公司 | 一种2-羟基-4-甲硫基丁腈的连续制备工艺和装置 |
| WO2025018942A1 (en) | 2023-07-17 | 2025-01-23 | Mojia Biotech Pte. Ltd. | Production of methionine via condensation of methional and c1-derived formyl-coa |
| CN119912370B (zh) * | 2025-04-03 | 2025-08-05 | 山东新和成氨基酸有限公司 | 一种2-羟基-4-甲硫基丁腈的制备方法及反应装置 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0649020A (ja) * | 1992-05-21 | 1994-02-22 | Daicel Chem Ind Ltd | 2−ヒドロキシ−4−メチルチオブタン酸の製造法 |
| JP2002503206A (ja) * | 1996-04-01 | 2002-01-29 | ユニオン カーバイド ケミカルズ アンド プラスティックス テクノロジー コーポレイション | メチルメルカプトプロパナールの製造方法 |
| JP2004115461A (ja) * | 2002-09-27 | 2004-04-15 | Sumitomo Chem Co Ltd | 3−メチルチオプロパナールの製造方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2542768A (en) * | 1945-10-24 | 1951-02-20 | Du Pont | Hydroxy-methylmercaptobutyronitrile |
| DE2320544C2 (de) | 1973-04-21 | 1975-06-05 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Verfahren zur Herstellung von 3-Methylmercaptopropionaldehyd |
| FR2314917A1 (fr) | 1975-06-20 | 1977-01-14 | Rhone Poulenc Ind | Procede de fabrication de l'aldehyde beta-methylthiopropionique |
| DE2623285C3 (de) | 1976-05-25 | 1980-10-02 | Gebrueder Grau Und Co Kg Chem. Fabrik, 7070 Schwaebisch Gmuend | Riechstoffkomposition |
| FR2460925A1 (fr) | 1979-07-10 | 1981-01-30 | Rhone Poulenc Ind | Procede de preparation directe d'aldehyde beta-methylthiopropionique |
| FR2480925A1 (fr) | 1980-04-22 | 1981-10-23 | Electricite De France | Echangeur thermique modulaire |
| US4440676A (en) | 1981-12-24 | 1984-04-03 | The British Petroleum Company P.L.C. | Process for the production of a dipeptide, a polypeptide or a protein |
| US5352837A (en) | 1993-06-08 | 1994-10-04 | Novus International, Inc. | Process for the preparation of 3-(methylthio)propanal |
| US5905171A (en) | 1995-06-22 | 1999-05-18 | Novus International, Inc. | Process for the preparation of 3-(methylthio)propanal |
| US5663409A (en) * | 1995-06-07 | 1997-09-02 | Novus International, Inc. | Process for the preparation of 3-(methylthio) propanal and 2-hydroxy-4-(methylthio) butanenitrile |
| AR002174A1 (es) * | 1995-06-07 | 1998-01-07 | Novus Int Inc | Proceso para la preparacion de 3-(metiltio)propanal y 2-hidroxi-4-metiltio) butanonitrilo |
| JP4517486B2 (ja) * | 2000-09-25 | 2010-08-04 | 住友化学株式会社 | 2−ヒドロキシ−4−メチルチオブタンニトリルの製造方法 |
| US20050038289A1 (en) | 2001-07-23 | 2005-02-17 | Gordon Richard S | Chemical reactions in compressed carbon dioxide |
-
2004
- 2004-08-05 DE DE102004038053A patent/DE102004038053A1/de not_active Ceased
-
2005
- 2005-07-14 RU RU2007108071/04A patent/RU2383531C2/ru not_active IP Right Cessation
- 2005-07-14 JP JP2007524209A patent/JP4773441B2/ja not_active Expired - Fee Related
- 2005-07-14 EP EP15186588.8A patent/EP2987785B1/de not_active Expired - Lifetime
- 2005-07-14 CN CN2005800265919A patent/CN101031542B/zh not_active Expired - Fee Related
- 2005-07-14 BR BRPI0513072-7A patent/BRPI0513072A/pt not_active Application Discontinuation
- 2005-07-14 ES ES15186588.8T patent/ES2667220T3/es not_active Expired - Lifetime
- 2005-07-14 EP EP05775924.3A patent/EP1778631B1/de not_active Expired - Lifetime
- 2005-07-14 CA CA002573047A patent/CA2573047A1/en not_active Abandoned
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- 2005-07-14 WO PCT/EP2005/007666 patent/WO2006015684A2/de not_active Ceased
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0649020A (ja) * | 1992-05-21 | 1994-02-22 | Daicel Chem Ind Ltd | 2−ヒドロキシ−4−メチルチオブタン酸の製造法 |
| JP2002503206A (ja) * | 1996-04-01 | 2002-01-29 | ユニオン カーバイド ケミカルズ アンド プラスティックス テクノロジー コーポレイション | メチルメルカプトプロパナールの製造方法 |
| JP2004115461A (ja) * | 2002-09-27 | 2004-04-15 | Sumitomo Chem Co Ltd | 3−メチルチオプロパナールの製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101031542B (zh) | 2010-05-12 |
| EP1778631A2 (de) | 2007-05-02 |
| WO2006015684A2 (de) | 2006-02-16 |
| BRPI0513072A (pt) | 2008-04-22 |
| CN101812004A (zh) | 2010-08-25 |
| JP2011132256A (ja) | 2011-07-07 |
| EP1778631B1 (de) | 2015-11-18 |
| CA2573047A1 (en) | 2006-02-16 |
| US7119233B2 (en) | 2006-10-10 |
| ES2667220T3 (es) | 2018-05-10 |
| MX2007000345A (es) | 2007-03-07 |
| EP2987785B1 (de) | 2018-03-14 |
| JP5306402B2 (ja) | 2013-10-02 |
| DE102004038053A1 (de) | 2006-04-27 |
| WO2006015684A3 (de) | 2006-08-03 |
| RU2007108071A (ru) | 2008-09-20 |
| CN101031542A (zh) | 2007-09-05 |
| CN101812004B (zh) | 2012-09-19 |
| RU2383531C2 (ru) | 2010-03-10 |
| EP2987785A1 (de) | 2016-02-24 |
| ES2560447T3 (es) | 2016-02-19 |
| JP2008508330A (ja) | 2008-03-21 |
| US20060030739A1 (en) | 2006-02-09 |
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