BE569344A - - Google Patents
Info
- Publication number
- BE569344A BE569344A BE569344DA BE569344A BE 569344 A BE569344 A BE 569344A BE 569344D A BE569344D A BE 569344DA BE 569344 A BE569344 A BE 569344A
- Authority
- BE
- Belgium
- Prior art keywords
- solvent
- alkyl
- mixture
- benzoic acid
- oxidation
- Prior art date
Links
- 239000002904 solvent Substances 0.000 claims description 26
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 12
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 8
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims description 8
- 230000003647 oxidation Effects 0.000 claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 8
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000005711 Benzoic acid Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000004151 quinonyl group Chemical group 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 125000005907 alkyl ester group Chemical group 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 4
- 238000000605 extraction Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 4
- 239000007868 Raney catalyst Substances 0.000 description 4
- 229910000564 Raney nickel Inorganic materials 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- HSKPJQYAHCKJQC-UHFFFAOYSA-N 1-ethylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2CC HSKPJQYAHCKJQC-UHFFFAOYSA-N 0.000 description 2
- -1 alkyl anthraquinone Chemical class 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- DUAYDERMVQWIJD-UHFFFAOYSA-N 2-n,2-n,6-trimethyl-1,3,5-triazine-2,4-diamine Chemical compound CN(C)C1=NC(C)=NC(N)=N1 DUAYDERMVQWIJD-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- KYZHGEFMXZOSJN-UHFFFAOYSA-N benzoic acid isobutyl ester Natural products CC(C)COC(=O)C1=CC=CC=C1 KYZHGEFMXZOSJN-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229940073644 nickel Drugs 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
- C01B15/01—Hydrogen peroxide
- C01B15/022—Preparation from organic compounds
- C01B15/023—Preparation from organic compounds by the alkyl-anthraquinone process
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE569344A true BE569344A (enrdf_load_stackoverflow) |
Family
ID=188340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE569344D BE569344A (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE569344A (enrdf_load_stackoverflow) |
-
0
- BE BE569344D patent/BE569344A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0275771B1 (fr) | Procédé de préparation des tétrahydro-1,1,2,2, perfluoroalcanols et de leurs esters | |
BE569344A (enrdf_load_stackoverflow) | ||
EP0024224A1 (fr) | Procédé de préparation des 1,1,2,2-tétrahydro perfluoro alcanols et des esters de ces alcools | |
EP0276605B1 (fr) | Synthèse des tetrahydro-1,1,2,2 perfluoroalcanols et de leurs esters | |
EP0288337A1 (fr) | Procédé d'oxydation de composés organiques par l'eau oxygénée en présence d'un catalyseur | |
CH328422A (fr) | Procédé de préparation d'un ester époxydé d'un acide aliphatique non saturé, insoluble dans l'eau | |
BE592385A (enrdf_load_stackoverflow) | ||
CH290882A (fr) | Procédé de préparation d'eau oxygénée par hydrogénation et oxydation d'au moins un composé contenant le groupement para-quinonique dissout dans un mélange de solvants. | |
CH329253A (fr) | Procédé d'époxydation | |
BE562814A (enrdf_load_stackoverflow) | ||
CH290883A (fr) | Procédé de préparation d'eau oxygénée par hydrogénation et oxydation d'anthraquinones alcoylées. | |
BE563806A (enrdf_load_stackoverflow) | ||
BE566625A (enrdf_load_stackoverflow) | ||
FR2465685A2 (fr) | Solutions d'anhydride borique et leur utilisation comme durcisseurs de resols | |
CH327271A (fr) | Procédé d'époxydation | |
BE452153A (enrdf_load_stackoverflow) | ||
BE592886A (enrdf_load_stackoverflow) | ||
BE624039A (enrdf_load_stackoverflow) | ||
BE498669A (enrdf_load_stackoverflow) | ||
BE531403A (enrdf_load_stackoverflow) | ||
BE522828A (enrdf_load_stackoverflow) | ||
BE455197A (enrdf_load_stackoverflow) | ||
BE485945A (enrdf_load_stackoverflow) | ||
CH326543A (fr) | Procédé pour préparer des vinyl-éthinyl-carbinols tertiaires | |
BE499222A (enrdf_load_stackoverflow) |