BE660638A - - Google Patents
Info
- Publication number
- BE660638A BE660638A BE660638A BE660638A BE660638A BE 660638 A BE660638 A BE 660638A BE 660638 A BE660638 A BE 660638A BE 660638 A BE660638 A BE 660638A BE 660638 A BE660638 A BE 660638A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- chlorinated
- chlorine
- vinyl compounds
- heterocyclic
- Prior art date
Links
- 239000000460 chlorine Substances 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000007789 gas Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000005660 chlorination reaction Methods 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- MLMGJTAJUDSUKA-UHFFFAOYSA-N 2-ethenyl-1h-imidazole Chemical compound C=CC1=NC=CN1 MLMGJTAJUDSUKA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- -1 nitrogenous heterocyclic compounds Chemical class 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- VDSAXHBDVIUOGV-UHFFFAOYSA-N 1-ethenyl-2-methyl-4,5-dihydroimidazole Chemical compound CC1=NCCN1C=C VDSAXHBDVIUOGV-UHFFFAOYSA-N 0.000 description 1
- NWHSSMRWECHZEP-UHFFFAOYSA-N 1-ethenylpyrazole Chemical compound C=CN1C=CC=N1 NWHSSMRWECHZEP-UHFFFAOYSA-N 0.000 description 1
- SRVJJBHJTKZCOC-UHFFFAOYSA-N 3-ethenyl-1,3-oxazolidine Chemical compound C=CN1CCOC1 SRVJJBHJTKZCOC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE660638A BE660638A (d) | 1965-03-04 | 1965-03-04 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE660638A BE660638A (d) | 1965-03-04 | 1965-03-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE660638A true BE660638A (d) | 1965-07-01 |
Family
ID=3847350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE660638A BE660638A (d) | 1965-03-04 | 1965-03-04 |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE660638A (d) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3404147A (en) * | 1964-01-28 | 1968-10-01 | Gaf Corp | Monohaloalkyl and polyhaloalkyl lactams |
-
1965
- 1965-03-04 BE BE660638A patent/BE660638A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3404147A (en) * | 1964-01-28 | 1968-10-01 | Gaf Corp | Monohaloalkyl and polyhaloalkyl lactams |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7799959B2 (en) | Process for producing 1,2,3,4-tetrachlorohexafluorobutane | |
| FR2552416A1 (fr) | Procede de preparation de trifluorure d'azote par reaction gaz-solide | |
| EP0298870B1 (fr) | Synthèse des bromures de perfluoroalkyle | |
| BE660638A (d) | ||
| EP3941902B1 (en) | A process for preparation of trifluoromethanesulfinyl chloride | |
| AU2003288184B2 (en) | Process for the preparation of 2,6-dihalo-para-trifluoromethylaniline | |
| EP0499516B1 (fr) | Synthèse d'hydrogéno-perfluoroalcanes | |
| EP0199661B1 (fr) | Procédé de préparation d'acylbiphényles | |
| CA1160646A (en) | Process for the selective aliphatic chlorination of alkylbenzenes | |
| EP1165483B1 (fr) | Procede de preparation du fluorure de carbonyle | |
| EP1140785B1 (fr) | Procede de preparation de para-trifluoromethylanilines polyhalogenees | |
| CA1283420C (fr) | Procede de synthese du n-amino aza-3 bicyclo ¬3,3,0|octane | |
| CA1280124C (fr) | Procede de preparation de 4-fluoroanilines a partir de 4-halogenonitrobenzenes | |
| FR2463745A1 (fr) | Procede pour preparer le sulfure de carbonyle | |
| EP0515258B1 (fr) | Synthèse de bromures de perfluoroalkyle | |
| EP0842136B1 (fr) | Procede de preparation d'alpha,omega-bromochloroalcanes | |
| FR2602764A1 (fr) | Composes dichlorotrifluoromethyltoluenes et procede de preparation de ces composes | |
| FR2472552A1 (fr) | Procede de production de 1,3,5-trichlorobenzene par chloration d'un trihalobenzene en phase vapeur | |
| EP0305288B1 (fr) | Procédé d'élimination du chlore | |
| EP0549387A1 (fr) | Synthèse du bromure de n.perfluorooctyle | |
| FR2627180A1 (fr) | Hydrocarbures chlorofluores et leur procede de preparation | |
| JPH06316404A (ja) | クロラミンの製造方法 | |
| BE624397A (d) | ||
| JPH11322645A (ja) | シクロアルケンの塩素化方法 | |
| JPH02258741A (ja) | ２―クロルテレフタロイルクロライドの製法 |