IL28998A - Carbohydrate oxidation in the presence of boron compounds - Google Patents
Carbohydrate oxidation in the presence of boron compoundsInfo
- Publication number
- IL28998A IL28998A IL28998A IL2899867A IL28998A IL 28998 A IL28998 A IL 28998A IL 28998 A IL28998 A IL 28998A IL 2899867 A IL2899867 A IL 2899867A IL 28998 A IL28998 A IL 28998A
- Authority
- IL
- Israel
- Prior art keywords
- oxidation
- boron
- hydrocarbon
- effluent
- adjuvant
- Prior art date
Links
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 93
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 90
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 84
- 230000003647 oxidation Effects 0.000 title claims abstract description 80
- 150000001875 compounds Chemical class 0.000 title abstract description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 81
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 73
- 229910052796 boron Inorganic materials 0.000 claims abstract description 73
- 239000002671 adjuvant Substances 0.000 claims abstract description 55
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 34
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims abstract description 21
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 15
- 239000007791 liquid phase Substances 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 9
- 239000012071 phase Substances 0.000 claims abstract description 6
- 239000003208 petroleum Substances 0.000 claims abstract description 5
- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical compound C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000004429 atom Chemical group 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 18
- -1 alicyclic hydrocarbon Chemical class 0.000 claims description 14
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims description 13
- 230000008569 process Effects 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000010924 continuous production Methods 0.000 claims description 3
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 11
- 239000011541 reaction mixture Substances 0.000 abstract description 11
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract description 10
- 150000002576 ketones Chemical class 0.000 abstract description 4
- 150000001298 alcohols Chemical class 0.000 abstract description 3
- 230000007062 hydrolysis Effects 0.000 abstract description 3
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 abstract description 2
- 241001292396 Cirrhitidae Species 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 34
- VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 description 14
- 235000010338 boric acid Nutrition 0.000 description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229960002645 boric acid Drugs 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 150000001639 boron compounds Chemical class 0.000 description 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 125000005619 boric acid group Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- BOOITXALNJLNMB-UHFFFAOYSA-N tricyclohexyl borate Chemical compound C1CCCCC1OB(OC1CCCCC1)OC1CCCCC1 BOOITXALNJLNMB-UHFFFAOYSA-N 0.000 description 3
- XDVOLDOITVSJGL-UHFFFAOYSA-N 3,7-dihydroxy-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B(O)OB2OB(O)OB1O2 XDVOLDOITVSJGL-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 150000001638 boron Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- FGGJBCRKSVGDPO-UHFFFAOYSA-N hydroperoxycyclohexane Chemical compound OOC1CCCCC1 FGGJBCRKSVGDPO-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000004977 peroxyborates Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 101150068888 MET3 gene Proteins 0.000 description 1
- 101100022915 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cys-11 gene Proteins 0.000 description 1
- 101100022918 Schizosaccharomyces pombe (strain 972 / ATCC 24843) sua1 gene Proteins 0.000 description 1
- 208000036366 Sensation of pressure Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 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
- C07C29/48—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
- C07C29/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
- C07C29/52—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only in the presence of mineral boron compounds with, when necessary, hydrolysis of the intermediate formed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered
- C07C2601/20—Systems containing only non-condensed rings with a ring being at least seven-membered the ring being twelve-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59661466A | 1966-11-23 | 1966-11-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL28998A true IL28998A (en) | 1971-07-28 |
Family
ID=24387992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL28998A IL28998A (en) | 1966-11-23 | 1967-11-22 | Carbohydrate oxidation in the presence of boron compounds |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3488740A (cs) |
| JP (1) | JPS5239023B1 (cs) |
| BE (1) | BE706822A (cs) |
| CH (1) | CH478736A (cs) |
| DE (1) | DE1668222A1 (cs) |
| ES (1) | ES347523A1 (cs) |
| FR (1) | FR1554787A (cs) |
| GB (1) | GB1210673A (cs) |
| IL (1) | IL28998A (cs) |
| LU (1) | LU54918A1 (cs) |
| NL (1) | NL6715611A (cs) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2044461C3 (de) * | 1970-09-08 | 1985-10-24 | Furman, Mendel Simchovič, Moskva | Verfahren zur mehrstufigen Oxydation von Cyclohexan |
| US3932513A (en) * | 1971-02-05 | 1976-01-13 | Halcon International, Inc. | Cyclohexane oxidation |
| DE19848730A1 (de) * | 1998-10-22 | 2000-04-27 | Degussa | Verfahren zur Herstellung cyclischer Alkohole |
| JP5526555B2 (ja) * | 2009-02-12 | 2014-06-18 | 住友化学株式会社 | シクロアルカノール及び／又はシクロアルカノンの製造方法 |
| US10479748B2 (en) | 2017-11-30 | 2019-11-19 | Cambridge Enterprise Limited | Oxidation of C1-9-alkanes |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1947989A (en) * | 1928-06-20 | 1934-02-20 | Firm A Riebeck Sche Montanwerk | Method of oxidizing hydrocarbons |
| US3317581A (en) * | 1964-01-17 | 1967-05-02 | Halcon International Inc | Hydrocarbon oxidation process to produce borate ester |
-
1966
- 1966-11-23 US US596614A patent/US3488740A/en not_active Expired - Lifetime
-
1967
- 1967-11-16 NL NL6715611A patent/NL6715611A/xx unknown
- 1967-11-20 GB GB52594/67A patent/GB1210673A/en not_active Expired
- 1967-11-21 LU LU54918D patent/LU54918A1/xx unknown
- 1967-11-21 BE BE706822D patent/BE706822A/xx not_active IP Right Cessation
- 1967-11-22 FR FR1554787D patent/FR1554787A/fr not_active Expired
- 1967-11-22 JP JP42074826A patent/JPS5239023B1/ja active Pending
- 1967-11-22 IL IL28998A patent/IL28998A/en unknown
- 1967-11-22 CH CH1639667A patent/CH478736A/fr not_active IP Right Cessation
- 1967-11-23 ES ES347523A patent/ES347523A1/es not_active Expired
- 1967-11-23 DE DE19671668222 patent/DE1668222A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US3488740A (en) | 1970-01-06 |
| JPS5239023B1 (cs) | 1977-10-03 |
| DE1668222A1 (de) | 1971-09-09 |
| GB1210673A (en) | 1970-10-28 |
| LU54918A1 (cs) | 1969-07-07 |
| CH478736A (fr) | 1969-09-30 |
| FR1554787A (cs) | 1969-01-24 |
| BE706822A (fr) | 1968-05-21 |
| ES347523A1 (es) | 1969-02-01 |
| NL6715611A (cs) | 1968-05-24 |
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