GB1047389A - - Google Patents
Info
- Publication number
- GB1047389A GB1047389A GB1047389DA GB1047389A GB 1047389 A GB1047389 A GB 1047389A GB 1047389D A GB1047389D A GB 1047389DA GB 1047389 A GB1047389 A GB 1047389A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bromoethyl
- alkyl
- tin
- bis
- ether
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- -1 Alkyl tin oxides Chemical class 0.000 abstract 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 150000003512 tertiary amines Chemical class 0.000 abstract 2
- 229910001887 tin oxide Inorganic materials 0.000 abstract 2
- GTQHJCOHNAFHRE-UHFFFAOYSA-N 1,10-dibromodecane Chemical compound BrCCCCCCCCCCBr GTQHJCOHNAFHRE-UHFFFAOYSA-N 0.000 abstract 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 1
- VEFLKXRACNJHOV-UHFFFAOYSA-N 1,3-dibromopropane Chemical compound BrCCCBr VEFLKXRACNJHOV-UHFFFAOYSA-N 0.000 abstract 1
- IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical compound BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 abstract 1
- YYWACUFAVLSCPF-UHFFFAOYSA-N 1-bromo-2-(2-bromoethylsulfanyl)ethane Chemical compound BrCCSCCBr YYWACUFAVLSCPF-UHFFFAOYSA-N 0.000 abstract 1
- JASUZIAETLGSCB-UHFFFAOYSA-N 1-bromo-2-(2-bromoethylsulfonyl)ethane Chemical compound BrCCS(=O)(=O)CCBr JASUZIAETLGSCB-UHFFFAOYSA-N 0.000 abstract 1
- MMYKTRPLXXWLBC-UHFFFAOYSA-N 1-bromo-2-ethoxyethane Chemical compound CCOCCBr MMYKTRPLXXWLBC-UHFFFAOYSA-N 0.000 abstract 1
- ZPHGARLYQHMNTB-UHFFFAOYSA-N 2-(2-chloroethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCl)C(=O)C2=C1 ZPHGARLYQHMNTB-UHFFFAOYSA-N 0.000 abstract 1
- 125000005999 2-bromoethyl group Chemical group 0.000 abstract 1
- RQFUZUMFPRMVDX-UHFFFAOYSA-N 3-Bromo-1-propanol Chemical compound OCCCBr RQFUZUMFPRMVDX-UHFFFAOYSA-N 0.000 abstract 1
- WJEZEUJKYFXNKJ-UHFFFAOYSA-N 4-(2-bromoethyl)benzaldehyde Chemical compound BrCCC1=CC=C(C=O)C=C1 WJEZEUJKYFXNKJ-UHFFFAOYSA-N 0.000 abstract 1
- JLOWNBACZCLCEP-UHFFFAOYSA-N 4-bromo-n,n-dimethylbutan-1-amine Chemical compound CN(C)CCCCBr JLOWNBACZCLCEP-UHFFFAOYSA-N 0.000 abstract 1
- HTKABMPGOHRVCT-UHFFFAOYSA-N 5-bromopentan-2-one Chemical compound CC(=O)CCCBr HTKABMPGOHRVCT-UHFFFAOYSA-N 0.000 abstract 1
- 239000002879 Lewis base Substances 0.000 abstract 1
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical compound CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 abstract 1
- 125000000524 functional group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 150000004679 hydroxides Chemical class 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 150000007527 lewis bases Chemical class 0.000 abstract 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 abstract 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000001174 sulfone group Chemical group 0.000 abstract 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/12—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing tin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4627763 | 1963-11-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1047389A true GB1047389A (enrdf_load_stackoverflow) | 1900-01-01 |
Family
ID=10440581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1047389D Expired GB1047389A (enrdf_load_stackoverflow) | 1963-11-22 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1047389A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2225322A1 (de) * | 1972-05-25 | 1973-12-20 | Ciba Geigy Marienberg Gmbh | Verfahren zur herstellung von organozinnhalogeniden in sulfonen als reaktionsmedium |
| US3954820A (en) | 1974-02-19 | 1976-05-04 | Ferro Corporation | Preparation of hydrocarbyl metal halides |
| US3970679A (en) | 1972-05-25 | 1976-07-20 | Ciba-Geigy Corporation | Process for the production of organotin halides in sulphones as reaction medium |
-
0
- GB GB1047389D patent/GB1047389A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2225322A1 (de) * | 1972-05-25 | 1973-12-20 | Ciba Geigy Marienberg Gmbh | Verfahren zur herstellung von organozinnhalogeniden in sulfonen als reaktionsmedium |
| US3970679A (en) | 1972-05-25 | 1976-07-20 | Ciba-Geigy Corporation | Process for the production of organotin halides in sulphones as reaction medium |
| US3954820A (en) | 1974-02-19 | 1976-05-04 | Ferro Corporation | Preparation of hydrocarbyl metal halides |
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