SU249629A1 - - Google Patents
Info
- Publication number
- SU249629A1 SU249629A1 SU1255465A SU1255465A SU249629A1 SU 249629 A1 SU249629 A1 SU 249629A1 SU 1255465 A SU1255465 A SU 1255465A SU 1255465 A SU1255465 A SU 1255465A SU 249629 A1 SU249629 A1 SU 249629A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- furyl
- furfural
- amount
- fulvene
- ethyl
- Prior art date
Links
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 239000011347 resin Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- PGTKVMVZBBZCKQ-UHFFFAOYSA-N Fulvene Chemical class C=C1C=CC=C1 PGTKVMVZBBZCKQ-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000002541 furyl group Chemical group 0.000 description 3
- -1 1-furyl-2-ethyl Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- HRYYXFYLNRICQD-UHFFFAOYSA-N 5-butan-2-ylidenecyclopenta-1,3-diene Chemical compound CCC(C)=C1C=CC=C1 HRYYXFYLNRICQD-UHFFFAOYSA-N 0.000 description 1
- WXACXMWYHXOSIX-UHFFFAOYSA-N 5-propan-2-ylidenecyclopenta-1,3-diene Chemical compound CC(C)=C1C=CC=C1 WXACXMWYHXOSIX-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU249629A1 true SU249629A1 (enExample) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3856833A (en) | Method for the production of aldehydic acids | |
| SU505357A3 (ru) | Способ получени 3-метилмеркаптопропионового альдегида | |
| SU249629A1 (enExample) | ||
| JP5827694B2 (ja) | アルジトールアセタールの製造方法 | |
| SU267068A1 (ru) | Способ получения смол на основе циклопентадиена | |
| US2662919A (en) | Hydrolysis of alkenyl alkyl ethers in the vapor phase | |
| CN114605375A (zh) | 一种2-噻吩乙酸的合成方法 | |
| US2484499A (en) | Process for preparing ester lactones | |
| SU202929A1 (ru) | Способ получения винилциклогексана | |
| US2759979A (en) | Manufacture of aldehydes by the pyrolysis of acetals | |
| SU188505A1 (enExample) | ||
| JPS5849327A (ja) | オルトヒドロキシベンジルアルコ−ル類の製法 | |
| US2673219A (en) | Manufacture of pimelic acid | |
| SU162153A1 (enExample) | ||
| SU166712A1 (ru) | Способ получения фурилалканонов-3 | |
| SU188511A1 (enExample) | ||
| SU168445A1 (enExample) | ||
| SU125800A1 (ru) | Способ получени ацетата v1v - диметилаллилового спирта | |
| SU447031A1 (ru) | Способ получени , -диалкил-2,6-динитро , , -трифтор-п-толуидинов | |
| SU196044A1 (enExample) | ||
| SU146036A1 (ru) | Способ получени мономерных соединений из производных фурфурола и кетонов | |
| SU278112A1 (ru) | Способ получения полимеров диалкиловых эфиров р-замещенной винилфосфиновой кислоты | |
| SU490800A1 (ru) | Способ получени 2-фенилбензимидазола | |
| JPS58152844A (ja) | トリアリ−ルメタン誘導体の製造方法 | |
| SU190897A1 (ru) | Способ получения органил- |