BE515078A - - Google Patents
Info
- Publication number
- BE515078A BE515078A BE515078DA BE515078A BE 515078 A BE515078 A BE 515078A BE 515078D A BE515078D A BE 515078DA BE 515078 A BE515078 A BE 515078A
- Authority
- BE
- Belgium
- Prior art keywords
- propylene
- chlorine
- chlorohydrin
- water
- solution
- Prior art date
Links
- 239000000460 chlorine Substances 0.000 claims description 31
- 229910052801 chlorine Inorganic materials 0.000 claims description 31
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 30
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 26
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 26
- 238000006243 chemical reaction Methods 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- VZIQXGLTRZLBEX-UHFFFAOYSA-N 2-chloro-1-propanol Chemical compound CC(Cl)CO VZIQXGLTRZLBEX-UHFFFAOYSA-N 0.000 claims description 11
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 6
- 238000010924 continuous production Methods 0.000 claims description 5
- 239000011261 inert gas Substances 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 description 20
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 239000007789 gas Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 7
- 239000006227 byproduct Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 150000003840 hydrochlorides Chemical class 0.000 description 3
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- ZEOVXNVKXIPWMS-UHFFFAOYSA-N 2,2-dichloropropane Chemical compound CC(C)(Cl)Cl ZEOVXNVKXIPWMS-UHFFFAOYSA-N 0.000 description 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/64—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens
- C07C29/66—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens by addition of hypohalogenous acids, which may be formed in situ, to carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE515078A true BE515078A (https=) |
Family
ID=152702
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE515078D BE515078A (https=) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE515078A (https=) |
-
0
- BE BE515078D patent/BE515078A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO337335B1 (no) | Fremgangsmåte for fremstilling av hydrogenperoksyd | |
| FR2824558A1 (fr) | Procede de fabrication d'un oxiranne | |
| EP0194931A1 (fr) | Procédé et appareil pour la sulfochloration photochimique d'alcanes gazeux | |
| CA1224807A (fr) | Procede de fabrication de nitromethane et installation | |
| FR2902787A1 (fr) | Procede de fabrication de 1,2-dichloroethane | |
| BE515078A (https=) | ||
| CA1161063A (fr) | Fabrication de chlorures d'alcane sulfonyles | |
| EP3814311A1 (fr) | Procédé de production du 1-chloro-3,3,3-trifluoropropène | |
| FR3009554A1 (fr) | Procede d'hydrobromuration | |
| FR2757500A1 (fr) | Procede de fabrication de bioxyde de chlore | |
| EP0277267B1 (fr) | Procédé de synthèse du N-amino aza-3 bicyclo [3,3,0] octane | |
| CA1282432C (fr) | Procede de deshydrochloration en phase liquide d'halogenoalcanes en presence d'un initiateur a base de produit chlore organique | |
| US20060096869A1 (en) | Apparatus and process for the synthesis of hydrogen peroxide directly from hydrogen and oxygen | |
| FR2876373A1 (fr) | Procede d'oxydation par l'oxygene d'hydrocarbures cycliques satures | |
| WO2020216735A1 (fr) | Procede de preparation du bis(fluorosulfonyle) imide | |
| BE672580A (https=) | ||
| FR2880019A1 (fr) | Procede de fabrication de 1,2-dichloroethane | |
| CH389147A (fr) | Procédé de stabilisation d'acétylène gazeux sous pression | |
| BE586311A (https=) | ||
| FR2499068A1 (fr) | Procede de preparation des hypohalogenites de tert-alkyle | |
| CH295388A (fr) | Procédé de fabrication du bioxyde de chlore. | |
| EP0272945B1 (fr) | Procédé catalytique de carbonylation des alcanes | |
| BE474905A (https=) | ||
| FR2495138A1 (fr) | Procede de preparation de l'acide gloxylique | |
| CH525171A (fr) | Procédé pour l'obtention de l'hexachlorocyclohexane |