SU453838A3 - Способ получения двухъядерных гетероциклических спиртов - Google Patents
Способ получения двухъядерных гетероциклических спиртовInfo
- Publication number
- SU453838A3 SU453838A3 SU1821046A SU1821046A SU453838A3 SU 453838 A3 SU453838 A3 SU 453838A3 SU 1821046 A SU1821046 A SU 1821046A SU 1821046 A SU1821046 A SU 1821046A SU 453838 A3 SU453838 A3 SU 453838A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- mol
- product
- calculated
- mass
- mixture
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 9
- 150000001298 alcohols Chemical class 0.000 title 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 33
- 239000000047 product Substances 0.000 description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000001228 spectrum Methods 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000000155 melt Substances 0.000 description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 5
- 239000001103 potassium chloride Substances 0.000 description 5
- 235000011164 potassium chloride Nutrition 0.000 description 5
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 238000013467 fragmentation Methods 0.000 description 3
- 238000006062 fragmentation reaction Methods 0.000 description 3
- 238000001819 mass spectrum Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 150000001793 charged compounds Chemical class 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- -1 heterocyclic alcohols Chemical class 0.000 description 2
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 2
- 229940091173 hydantoin Drugs 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 230000005415 magnetization Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 235000021395 porridge Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000012264 purified product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- JTTFXYHJDZZDQK-UHFFFAOYSA-N 1,3-diazaspiro[4.4]nonane-2,4-dione Chemical compound N1C(=O)NC(=O)C11CCCC1 JTTFXYHJDZZDQK-UHFFFAOYSA-N 0.000 description 1
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- VSJRBQDMBFFHMC-UHFFFAOYSA-N 5-ethyl-5-methylimidazolidine-2,4-dione Chemical compound CCC1(C)NC(=O)NC1=O VSJRBQDMBFFHMC-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000001321 HNCO Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- 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
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/26—Di-epoxy compounds heterocyclic
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3236—Heterocylic compounds
- C08G59/3245—Heterocylic compounds containing only nitrogen as a heteroatom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epoxy Resins (AREA)
- Epoxy Compounds (AREA)
- Organic Insulating Materials (AREA)
- Reinforced Plastic Materials (AREA)
- Paints Or Removers (AREA)
- Furan Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH539871A CH550820A (de) | 1971-04-14 | 1971-04-14 | Verfahren zur herstellung von heterocyclischen triglycidylverbindungen. |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU45035A Addition SU23325A1 (ru) | 1929-04-15 | 1929-04-15 | Гвоздильный станок двойного действи |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU453838A3 true SU453838A3 (ru) | 1974-12-15 |
Family
ID=4292898
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1821046A SU453838A3 (ru) | 1971-04-14 | 1972-04-12 | Способ получения двухъядерных гетероциклических спиртов |
| SU1826233A SU509242A3 (ru) | 1971-04-14 | 1972-04-12 | Самоотверждающа с смесь |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1826233A SU509242A3 (ru) | 1971-04-14 | 1972-04-12 | Самоотверждающа с смесь |
Country Status (19)
| Country | Link |
|---|---|
| JP (3) | JPS5644090B1 (enExample) |
| AR (2) | AR194476A1 (enExample) |
| AT (1) | AT318922B (enExample) |
| AU (1) | AU469852B2 (enExample) |
| BE (1) | BE782032A (enExample) |
| BR (2) | BR7202217D0 (enExample) |
| CA (1) | CA993445A (enExample) |
| CH (1) | CH550820A (enExample) |
| DD (3) | DD105246A5 (enExample) |
| DE (1) | DE2217914A1 (enExample) |
| ES (1) | ES411737A1 (enExample) |
| FR (2) | FR2155193A5 (enExample) |
| GB (1) | GB1380602A (enExample) |
| IT (1) | IT957186B (enExample) |
| NL (1) | NL7204979A (enExample) |
| RO (1) | RO67634B (enExample) |
| SE (2) | SE389867B (enExample) |
| SU (2) | SU453838A3 (enExample) |
| ZA (2) | ZA727802B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH635604A5 (de) * | 1978-06-22 | 1983-04-15 | Ciba Geigy Ag | Mischung auf basis eines haertbaren epoxidharzes, eines haerters dafuer und eines haertungsbeschleunigers. |
| US4210744A (en) * | 1978-12-11 | 1980-07-01 | Ciba-Geigy Corporation | Adducts containing epoxide groups, from hydantoin trisepoxides and binuclear hydantoins |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2809942A (en) * | 1955-10-21 | 1957-10-15 | Devoe & Raynolds Co | Process for making polyglycidyl cyanurates |
| NL218410A (enExample) * | 1956-06-26 | |||
| FR1394438A (fr) * | 1964-04-22 | 1965-04-02 | Akad Wissenschaften Ddr | Procédé de production d'isocyanurates de triglycidyle monomères |
| DE1932305A1 (de) * | 1968-09-13 | 1970-03-19 | Akad Wissenschaften Ddr | Verfahren zur Herstellung von Epoxydharzformstoffen |
| DE1932306A1 (de) * | 1968-09-13 | 1970-03-19 | Akad Wissenschaften Ddr | Verfahren zur Herstellung von N-Glykoluril-Derivaten |
-
1971
- 1971-04-14 CH CH539871A patent/CH550820A/xx not_active IP Right Cessation
-
1972
- 1972-03-14 CA CA137,006A patent/CA993445A/en not_active Expired
- 1972-03-16 AU AU40083/72A patent/AU469852B2/en not_active Expired
- 1972-03-23 SE SE7203760A patent/SE389867B/xx unknown
- 1972-04-06 GB GB1599372A patent/GB1380602A/en not_active Expired
- 1972-04-11 JP JP3581372A patent/JPS5644090B1/ja active Pending
- 1972-04-12 SU SU1821046A patent/SU453838A3/ru active
- 1972-04-12 IT IT7244/72A patent/IT957186B/it active
- 1972-04-12 AR AR241428A patent/AR194476A1/es active
- 1972-04-12 SU SU1826233A patent/SU509242A3/ru active
- 1972-04-13 DE DE19722217914 patent/DE2217914A1/de not_active Withdrawn
- 1972-04-13 ZA ZA727802*A patent/ZA727802B/xx unknown
- 1972-04-13 DD DD172373*A patent/DD105246A5/xx unknown
- 1972-04-13 BE BE782032A patent/BE782032A/xx unknown
- 1972-04-13 DD DD162275A patent/DD101408A5/xx unknown
- 1972-04-13 DD DD172369*A patent/DD106379A5/xx unknown
- 1972-04-13 FR FR7212972A patent/FR2155193A5/fr not_active Expired
- 1972-04-13 AT AT322772A patent/AT318922B/de not_active IP Right Cessation
- 1972-04-13 NL NL7204979A patent/NL7204979A/xx not_active Application Discontinuation
- 1972-04-13 ZA ZA722483A patent/ZA722483B/xx unknown
- 1972-04-14 RO RO74598A patent/RO67634B/ro unknown
- 1972-04-14 BR BR722217A patent/BR7202217D0/pt unknown
- 1972-10-11 BR BR007078/72A patent/BR7207078D0/pt unknown
- 1972-11-30 FR FR7242601A patent/FR2163160A5/fr not_active Expired
-
1973
- 1973-01-01 AR AR248823A patent/AR204615A1/es active
- 1973-02-17 ES ES411737A patent/ES411737A1/es not_active Expired
-
1974
- 1974-09-17 SE SE7411680-7A patent/SE407684B/xx not_active IP Right Cessation
-
1980
- 1980-08-09 JP JP55109757A patent/JPS58419B2/ja not_active Expired
-
1982
- 1982-05-04 JP JP57075063A patent/JPS5855150B2/ja not_active Expired
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