SU237147A1 - - Google Patents

Info

Publication number

SU237147A1

SU237147A1 SU1200954A SU1200954A SU237147A1 SU 237147 A1 SU237147 A1 SU 237147A1 SU 1200954 A SU1200954 A SU 1200954A SU 1200954 A SU1200954 A SU 1200954A SU 237147 A1 SU237147 A1 SU 237147A1

Authority

SU

USSR - Soviet Union

Prior art keywords

acid

mol

methacrylic acid

acrylic

triethylamine

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
• CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
• SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
• 150000008064 anhydrides Chemical class 0.000 description 4
• 239000000047 product Substances 0.000 description 4
• 239000002253 acid Substances 0.000 description 3
• NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• -1 alkyl chlorophosphonate Chemical compound 0.000 description 2
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
• 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
• 239000007788 liquid Substances 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• 238000000034 method Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• 150000007513 acids Chemical class 0.000 description 1
• 125000005907 alkyl ester group Chemical group 0.000 description 1
• 150000005215 alkyl ethers Chemical class 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 238000004821 distillation Methods 0.000 description 1
• 239000000706 filtrate Substances 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 125000005395 methacrylic acid group Chemical group 0.000 description 1
• MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 239000000725 suspension Substances 0.000 description 1
• ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1