BE382869A - - Google Patents
Info
- Publication number
- BE382869A BE382869A BE382869DA BE382869A BE 382869 A BE382869 A BE 382869A BE 382869D A BE382869D A BE 382869DA BE 382869 A BE382869 A BE 382869A
- Authority
- BE
- Belgium
- Prior art keywords
- hydrochloric acid
- residue
- vinyl compound
- weight
- aromatic
- Prior art date
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 15
- -1 aromatic vinyl compound Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 238000001311 chemical methods and process Methods 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 19
- 238000003756 stirring Methods 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- ZMXIYERNXPIYFR-UHFFFAOYSA-N 1-ethylnaphthalene Chemical class C1=CC=C2C(CC)=CC=CC2=C1 ZMXIYERNXPIYFR-UHFFFAOYSA-N 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N o-xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229940108066 Coal Tar Drugs 0.000 description 1
- 210000004940 Nucleus Anatomy 0.000 description 1
- SBYMUDUGTIKLCR-VOTSOKGWSA-N [(E)-2-chloroethenyl]benzene Chemical compound Cl\C=C\C1=CC=CC=C1 SBYMUDUGTIKLCR-VOTSOKGWSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000003034 coal gas Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/08—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE382869A true BE382869A (hu) |
Family
ID=52172
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE382869D BE382869A (hu) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE382869A (hu) |
-
0
- BE BE382869D patent/BE382869A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2277895C (fr) | Compositions a base de dimethyldisulfure a odeur masquee | |
US2484841A (en) | Reduction of hydroperoxides | |
CH392496A (fr) | Procédé de préparation de diméthyl-1,1 indanes alcoylés | |
BE382869A (hu) | ||
BE498176A (hu) | ||
FR2546162A1 (fr) | Procede pour la preparation de 1,8-dihydroxy-10-acyl-9-anthrones, en particulier pour une utilisation dans le traitement du psoriasis | |
FR2510991A1 (fr) | Procede pour la preparation de methacrylamides et d'acrylamides n-substitues | |
CH622425A5 (hu) | ||
EP0403331B1 (fr) | Procédé de séparation de deux isomères, son application à la purification du phényl-1 bromo-2 éthane | |
FR2673189A1 (fr) | Utilisation d'isomeres de mono et bis(methylbenzyl)xylene comme fluide de transfert technique. | |
EP1268374A1 (fr) | Compositions de mono- et polybenzyl-1,2,3,4-tetrahydronaphtalenes, utilisation desdites compositions ou d'un melange d'isomeres du monobenzyl-1,2,3,4-tetrahydronaphtalene comme fluide de transfert de chaleur | |
FR2545083A1 (fr) | Composition liquide, contenant des diisocyanates a structure diphenylmethane, et son procede de fabrication | |
EP0478428A2 (fr) | Procédé de préparation d'oxyde borique par hydrolyse du borate de méthyle et sa mise en oeuvre dans l'oxydation d'hydrocarbures saturées en alcools | |
FR2739376A1 (fr) | Procede de preparation du 2-chloro-4-methylphenol a partir du 4-methylphenol | |
US3019263A (en) | Process for preparing 1-acetyl-2, 2, 3-trimethylcyclobutane | |
BE555180A (hu) | ||
FR2618148A1 (fr) | Nouveau procede de preparation enantiospecifique du (s) ethylamino-2 (trifluoromethyl-3 phenyl)-1 propane | |
BE434734A (hu) | ||
BE487031A (hu) | ||
BE571721A (hu) | ||
BE449574A (hu) | ||
CH409932A (fr) | Procédé de préparation de chlorure de sulfényle chloré sur l'atome de Ca | |
BE529997A (hu) | ||
BE558730A (hu) | ||
BE563303A (hu) |