SU159505A1 - - Google Patents

Info

Publication number

SU159505A1

SU159505A1 SU802191A SU802191A SU159505A1 SU 159505 A1 SU159505 A1 SU 159505A1 SU 802191 A SU802191 A SU 802191A SU 802191 A SU802191 A SU 802191A SU 159505 A1 SU159505 A1 SU 159505A1

Authority

SU

USSR - Soviet Union

Prior art keywords

acetate

ketospirits

esters

furyl

mercury

Prior art date

Links

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• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
• 238000000034 method Methods 0.000 description 5
• 150000002148 esters Chemical class 0.000 description 4
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
• 125000001931 aliphatic group Chemical group 0.000 description 3
• 229910052739 hydrogen Inorganic materials 0.000 description 3
• 239000001257 hydrogen Substances 0.000 description 3
• QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
• 229910052753 mercury Inorganic materials 0.000 description 3
• 239000002994 raw material Substances 0.000 description 3
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• 150000001242 acetic acid derivatives Chemical class 0.000 description 2
• 239000003054 catalyst Substances 0.000 description 2
• 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
• 150000002240 furans Chemical class 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
• XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
• KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
• 229910052799 carbon Inorganic materials 0.000 description 1
• 239000003245 coal Substances 0.000 description 1
• 238000004821 distillation Methods 0.000 description 1
• 238000005984 hydrogenation reaction Methods 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000010453 quartz Substances 0.000 description 1
• 238000010992 reflux Methods 0.000 description 1
• 239000012047 saturated solution Substances 0.000 description 1
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 238000005809 transesterification reaction Methods 0.000 description 1

Cited By (1)