SU391129A1 - - Google Patents

Info

Publication number

SU391129A1

SU391129A1 SU1735274A SU1735274A SU391129A1 SU 391129 A1 SU391129 A1 SU 391129A1 SU 1735274 A SU1735274 A SU 1735274A SU 1735274 A SU1735274 A SU 1735274A SU 391129 A1 SU391129 A1 SU 391129A1

Authority

SU

USSR - Soviet Union

Prior art keywords

dimethoxybenzene

benzyl

dimethoxybenzenes

fraction

mol

Prior art date

1972-01-06

Links

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• OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 10
• 238000000034 method Methods 0.000 description 10
• 239000003054 catalyst Substances 0.000 description 5
• 150000005575 dimethoxybenzenes Chemical class 0.000 description 5
• SSDKWZABDIDDMO-UHFFFAOYSA-N 2-benzyl-1,4-dimethoxybenzene Chemical compound COC1=CC=C(OC)C(CC=2C=CC=CC=2)=C1 SSDKWZABDIDDMO-UHFFFAOYSA-N 0.000 description 4
• KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 4
• 229940073608 benzyl chloride Drugs 0.000 description 4
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
• 238000006243 chemical reaction Methods 0.000 description 4
• 239000000047 product Substances 0.000 description 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
• 238000004821 distillation Methods 0.000 description 3
• 230000015572 biosynthetic process Effects 0.000 description 2
• 239000001257 hydrogen Substances 0.000 description 2
• 229910052739 hydrogen Inorganic materials 0.000 description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 238000003786 synthesis reaction Methods 0.000 description 2
• SXUHHYZFGARGGI-UHFFFAOYSA-N 1,4-dibenzyl-2,5-dimethoxybenzene Chemical compound COC=1C=C(CC=2C=CC=CC=2)C(OC)=CC=1CC1=CC=CC=C1 SXUHHYZFGARGGI-UHFFFAOYSA-N 0.000 description 1
• LCQUULOIIXYZSJ-UHFFFAOYSA-N 4-[2-[4-[2-(4-hydroxyphenyl)ethyl]phenyl]ethyl]phenol Chemical compound C1=CC(O)=CC=C1CCC(C=C1)=CC=C1CCC1=CC=C(O)C=C1 LCQUULOIIXYZSJ-UHFFFAOYSA-N 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
• 239000003153 chemical reaction reagent Substances 0.000 description 1
• -1 dibenzyl-1,4-dimethoxybenzenes Chemical class 0.000 description 1
• 150000002148 esters Chemical class 0.000 description 1
• 239000012467 final product Substances 0.000 description 1
• 238000004817 gas chromatography Methods 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
• 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 239000000155 melt Substances 0.000 description 1
• 239000002304 perfume Substances 0.000 description 1
• 229920000642 polymer Polymers 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000011541 reaction mixture Substances 0.000 description 1
• 238000010992 reflux Methods 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1