BE667831A - - Google Patents
Info
- Publication number
- BE667831A BE667831A BE667831DA BE667831A BE 667831 A BE667831 A BE 667831A BE 667831D A BE667831D A BE 667831DA BE 667831 A BE667831 A BE 667831A
- Authority
- BE
- Belgium
- Prior art keywords
- phenol
- reaction
- acetone
- hydrochloric acid
- temperature
- Prior art date
Links
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 44
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 29
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 23
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 238000004821 distillation Methods 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 238000004508 fractional distillation Methods 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000001294 propane Substances 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 claims 1
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 13
- 229930185605 Bisphenol Natural products 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 7
- 238000005194 fractionation Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000010923 batch production Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000001577 simple distillation Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/74—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE667831 | 1965-08-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE667831A true BE667831A (enrdf_load_stackoverflow) | 1965-12-01 |
Family
ID=3847796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE667831D BE667831A (enrdf_load_stackoverflow) | 1965-08-03 | 1965-08-03 |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE667831A (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4517387A (en) * | 1982-09-30 | 1985-05-14 | Mitsui Petrochemical Industries, Ltd. | Process for production of 2,2-bis(4-hydroxyphenyl) propane |
-
1965
- 1965-08-03 BE BE667831D patent/BE667831A/fr unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4517387A (en) * | 1982-09-30 | 1985-05-14 | Mitsui Petrochemical Industries, Ltd. | Process for production of 2,2-bis(4-hydroxyphenyl) propane |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0751110B1 (fr) | Procédé de purification d'un flux gazeux contenant de l'acroléine | |
FR2862644A1 (fr) | Utilisation de ressources renouvelables | |
CA1062283A (fr) | Procede de cristallisation d'un complexe de di(hydroxy-4 phenyl)2,2 propane et de phenol | |
CA1169092A (fr) | PROCEDE POUR LA FABRICATION DE L'ACIDE .beta.- HYDROXYBUTYRIQUE ET DE SES OLIGOCONDENSATS | |
FR2467185A1 (fr) | Procedes de separation et de purification du resorcinol et de l'hydroquinone | |
BE667831A (enrdf_load_stackoverflow) | ||
EP4291547B1 (fr) | Procede perfectionne de fabrication d'acrylates d'alkyle de purete elevee | |
EP0121466B1 (fr) | Procédé de décomposition d'un complexe d'acide orthobenzoyl-benzoique, de fluorure d'hydrogène et de trifluorure de bore | |
EP0296990B1 (fr) | Procédé de fabrication de polybutadiène hydroxylé | |
JP3917201B2 (ja) | ビスフェノールaの製造方法 | |
JPS6127938A (ja) | ソルビン酸の製法 | |
BE1029670B1 (fr) | Procédé de récupération de lactide et d'acide lactique lors des étapes de production de polylactide (PLA) | |
FR2480277A1 (fr) | Procede pour isoler le monochloracetaldehyde | |
US3354054A (en) | Process for isolating and purifying 1-cyanobutadiene-(1, 3) by plural stage distillation in the presence of nitrogen oxide | |
US3817841A (en) | Separating adiponitrile from mixtures | |
BE678415A (enrdf_load_stackoverflow) | ||
US3328265A (en) | Process for the quantitative separation of formaldehyde from aqueous solutions by pressure distillation | |
WO2023025999A1 (fr) | Procede perfectionne de fabrication d'acrylate de butyle de purete elevee | |
FR2672065A1 (fr) | Procede pour la recuperation d'acides aliphatiques et de sucres a partir d'une solution epuisee de preparation de pate a papier. | |
BE555145A (enrdf_load_stackoverflow) | ||
CH325837A (fr) | Procédé de préparation de 1 : 1 :3-trialcoyloxyprop-2-ènes | |
KR20040106559A (ko) | 순수한 트리옥산의 제조 방법 | |
BE522886A (enrdf_load_stackoverflow) | ||
BE335350A (enrdf_load_stackoverflow) | ||
BE637024A (enrdf_load_stackoverflow) |