SU300991A1 - - Google Patents

Info

Publication number

SU300991A1

SU300991A1 SU1044892A SU1044892A SU300991A1 SU 300991 A1 SU300991 A1 SU 300991A1 SU 1044892 A SU1044892 A SU 1044892A SU 1044892 A SU1044892 A SU 1044892A SU 300991 A1 SU300991 A1 SU 300991A1

Authority

SU

USSR - Soviet Union

Prior art keywords

ether

propargyloxyphenoxy

propane

evaporated

dissolved

Prior art date

Links

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• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
• ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 5
• -1 o-propargyloxyphenoxy Chemical group 0.000 description 4
• 239000001294 propane Substances 0.000 description 4
• 150000003839 salts Chemical class 0.000 description 4
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
• OCDHRUIARWXIBR-UHFFFAOYSA-N 2-[(2-prop-2-ynoxyphenoxy)methyl]oxirane Chemical compound C#CCOC1=CC=CC=C1OCC1OC1 OCDHRUIARWXIBR-UHFFFAOYSA-N 0.000 description 2
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• 238000000034 method Methods 0.000 description 2
• 239000000243 solution Substances 0.000 description 2
• XSFWCIBEJZADAF-UHFFFAOYSA-N 2-prop-2-ynoxyphenol Chemical compound OC1=CC=CC=C1OCC#C XSFWCIBEJZADAF-UHFFFAOYSA-N 0.000 description 1
• 208000024172 Cardiovascular disease Diseases 0.000 description 1
• 235000010650 Hyssopus officinalis Nutrition 0.000 description 1
• 240000001812 Hyssopus officinalis Species 0.000 description 1
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
• 239000003929 acidic solution Substances 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 239000008346 aqueous phase Substances 0.000 description 1
• YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
• 239000012259 ether extract Substances 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 229940127554 medical product Drugs 0.000 description 1
• 239000000155 melt Substances 0.000 description 1
• 239000002245 particle Substances 0.000 description 1
• 230000000144 pharmacologic effect Effects 0.000 description 1
• 229940072033 potash Drugs 0.000 description 1
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
• 235000015320 potassium carbonate Nutrition 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 description 1
• 238000010992 reflux Methods 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1