DEC0005778MA - - Google Patents
Info
- Publication number
- DEC0005778MA DEC0005778MA DEC0005778MA DE C0005778M A DEC0005778M A DE C0005778MA DE C0005778M A DEC0005778M A DE C0005778MA
- Authority
- DE
- Germany
- Prior art keywords
- acid
- ester
- esterification
- vol
- yield
- 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.)
- Active
Links
- OFOBLEOULBTSOW-UHFFFAOYSA-N malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 18
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 16
- 238000005886 esterification reaction Methods 0.000 claims description 11
- MLIREBYILWEBDM-UHFFFAOYSA-N Cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 238000007127 saponification reaction Methods 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 6
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- FOCAUTSVDIKZOP-UHFFFAOYSA-N Chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- -1 diethyl ester Chemical class 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 235000002639 sodium chloride Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Diethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GWFWWCYVZMFJIV-UHFFFAOYSA-N [Ca].C(CC(=O)O)(=O)O Chemical compound [Ca].C(CC(=O)O)(=O)O GWFWWCYVZMFJIV-UHFFFAOYSA-N 0.000 description 2
- NLBFDFIZQKPFKP-UHFFFAOYSA-N [Na].C(#N)CC(=O)O Chemical compound [Na].C(#N)CC(=O)O NLBFDFIZQKPFKP-UHFFFAOYSA-N 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 239000011833 salt mixture Substances 0.000 description 2
- JAUCIKCNYHCSIR-UHFFFAOYSA-M sodium;2-cyanoacetate Chemical compound [Na+].[O-]C(=O)CC#N JAUCIKCNYHCSIR-UHFFFAOYSA-M 0.000 description 2
- 230000000576 supplementary Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N Ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- QIIGWXFEWHTAQM-WXXKFALUSA-N OC(=O)CCC(O)=O.OC(=O)\C=C\C(O)=O.OC(=O)C(O)C(O)C(O)=O Chemical compound OC(=O)CCC(O)=O.OC(=O)\C=C\C(O)=O.OC(=O)C(O)C(O)C(O)=O QIIGWXFEWHTAQM-WXXKFALUSA-N 0.000 description 1
- FDRCDNZGSXJAFP-UHFFFAOYSA-M Sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N Sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L cacl2 Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000011031 large scale production Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- QDHHCQZDFGDHMP-UHFFFAOYSA-N monochloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE60226229T2 (de) | Verfahren zur herstellung von carbonsäuren und deren derivaten | |
DE1793559C3 (de) | Verfahren zur Herstellung von Furan 3 carbonsaureestern Ausscheidung aus 1543804 | |
DE4114733A1 (de) | Verfahren zur herstellung von substituierten malonesteraniliden und malonsaeure-monoaniliden | |
DE2721264C2 (de) | Verfahren zur Herstellung von Di-n-propylessigsäure und deren nichttoxischen Alkali- und Erdalkalimetallsalzen | |
EP3655413B1 (fr) | Fabrication de glufosinate par conversion de 3-[n-butoxy(méthyl)phosphoryl]-1-cyanopropylacétate en une mélange de n-butyl(3-amino-3-cyanopropyl)-méthylphosphinate et la sel d'ammonium d'acid phosphinique (3-amino-3-cyanopropyl)-méthyl | |
DE3308922A1 (de) | Verfahren zur herstellung von fettsaeureestern der ascorbinsaeure | |
EP0087585A1 (fr) | Méthode de préparation de 3-alcoxi-acrylonitriles | |
DE2015840B2 (de) | Verfahren zur herstellung von fettsaeuredialkylamiden | |
DEC0005778MA (fr) | ||
EP0174624B1 (fr) | Procédé de préparation d'esters de l'acide lactique | |
DE953874C (de) | Verfahren zur Herstellung von Malonsaeurediaethylester | |
DE2404159C2 (de) | Verfahren zur Herstellung von 2-(4-Alkylphenyl)-propionsäuren und ihren Natrium-oder Kaliumsalzen | |
DE2721265C2 (de) | Verfahren zur Herstellung von Di- n-propylacetonitril | |
EP0879813B1 (fr) | Procédé de préparation d'acides cyclopropane carboxyliques | |
DE1643195C (fr) | ||
DE2936416C2 (fr) | ||
DE930686C (de) | Verfahren zur Herstellung von Dehydracetsaeure | |
DE1958619C3 (de) | Verfahren zur Herstellung substituierter Pyrazine | |
DE2060329C3 (de) | Verfahren zur Herstellung von substituierten Benzamiden | |
DE68907146T2 (de) | Verfahren zur Reinigung von D-hydroxyphenoxypropionsäure. | |
DE852994C (de) | Verfahren zur Herstellung von ª‰-Alkoxycarbonsaeureestern | |
DE969341C (de) | Verfahren zur Herstellung von Terephthalsaeuredimethylester | |
DE871751C (de) | Verfahren zur Gewinnung des Pentaerythrit-dichlorhydrinmonoschwefligsaeureesters | |
DE719571C (de) | Verfahren zur Herstellung von Aldehyden und Estern aus Aldehyddiacylaten | |
DE2606855C2 (de) | Verfahren zur Herstellung von Propionsäure-3,4-dichloranilid |