BE632193A - - Google Patents
Info
- Publication number
- BE632193A BE632193A BE632193DA BE632193A BE 632193 A BE632193 A BE 632193A BE 632193D A BE632193D A BE 632193DA BE 632193 A BE632193 A BE 632193A
- Authority
- BE
- Belgium
- Prior art keywords
- dimethyl
- dichloro
- pentane
- alkaline
- hydrochloric acid
- Prior art date
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 claims 1
- -1 ethylene glycidol Chemical compound 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- FKWZFRHUYPBHBJ-UHFFFAOYSA-N 1,5-dichloro-3,3-dimethylpentane Chemical compound ClCCC(C)(C)CCCl FKWZFRHUYPBHBJ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
- C07C1/30—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms by splitting-off the elements of hydrogen halide from a single molecule
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE632193A true BE632193A (enExample) |
Family
ID=200326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE632193D BE632193A (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE632193A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4579992A (en) * | 1983-08-25 | 1986-04-01 | Huels Aktiengesellschaft | Production of 3,3- and 2,3-dimethylbutenes, 2,3-dimethylbutadiene and/or glycol or polyglycol N-alkyl-3,3- and -2,3-dimethylbutyl ether |
-
0
- BE BE632193D patent/BE632193A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4579992A (en) * | 1983-08-25 | 1986-04-01 | Huels Aktiengesellschaft | Production of 3,3- and 2,3-dimethylbutenes, 2,3-dimethylbutadiene and/or glycol or polyglycol N-alkyl-3,3- and -2,3-dimethylbutyl ether |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS61286351A (ja) | シクロプロピルアミンの製造方法 | |
| BE632193A (enExample) | ||
| US2479283A (en) | Cyclic organic compounds | |
| JP2016538263A (ja) | フェノール性アルコールを調製するためのアルカンスルホン酸の使用 | |
| FR2466447A1 (fr) | Procede de preparation simultanee d'a,o-dialdehydes et d'a,o-diacides insatures ou satures et produits prepares selon ce procede | |
| EP0145618A2 (fr) | Procédé de préparation de la N,N'-bis(hydroxy-2 ethyl)oxamide | |
| RU2164509C1 (ru) | Способ получения 2,6-ди-трет-бутил-фенола | |
| CA1204123A (fr) | PROCEDE DE PREPARATION D'ACIDES MONOCARBOXYLIQUES DISUBSTITUES EN .alpha. ET DE LEURS ESTERS | |
| BE553772A (enExample) | ||
| BE457286A (enExample) | ||
| BE562435A (enExample) | ||
| BE626560A (enExample) | ||
| EP0373057A1 (fr) | Procédé de préparation de l'acide (propyl-2) pentène-2 oique et de ses esters | |
| CH180856A (fr) | Procédé de préparation de l'a-hexyl-cyclopentanone. | |
| BE443850A (enExample) | ||
| CH283425A (fr) | Procédé de préparation d'un produit odorant à partir de l'a-méthyl-furane. | |
| EP0301925A1 (fr) | Nouveau procédé de préparation énantiospécifique du (S) éthylamino-2 (trifluorométhyl-3 phényl)-1 propane | |
| BE627307A (enExample) | ||
| BE541295A (enExample) | ||
| CH288984A (fr) | Procédé de préparation d'un acylamidodiol aromatique, nitré dans le noyau. | |
| BE436566A (enExample) | ||
| BE380800A (enExample) | ||
| CH251641A (fr) | Procédé de fabrication de l'acétal dichloréthylique. | |
| BE335323A (enExample) | ||
| CH288991A (fr) | Procédé de préparation d'un acylamidodiol aromatique, nitré dans le noyau. |