ES378777A1 - Continuous method for the preparation of cumeno hydroperoxide. (Machine-translation by Google Translate, not legally binding) - Google Patents
Continuous method for the preparation of cumeno hydroperoxide. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES378777A1 ES378777A1 ES378777A ES378777A ES378777A1 ES 378777 A1 ES378777 A1 ES 378777A1 ES 378777 A ES378777 A ES 378777A ES 378777 A ES378777 A ES 378777A ES 378777 A1 ES378777 A1 ES 378777A1
- Authority
- ES
- Spain
- Prior art keywords
- oxygen
- cumene
- hydroperoxide
- moles
- per hour
- 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
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title abstract 2
- 238000011437 continuous method Methods 0.000 title 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 8
- 239000001301 oxygen Substances 0.000 abstract 8
- 229910052760 oxygen Inorganic materials 0.000 abstract 8
- 239000007789 gas Substances 0.000 abstract 4
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 230000003113 alkalizing effect Effects 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000010924 continuous production Methods 0.000 abstract 1
- 238000007701 flash-distillation Methods 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- 239000012263 liquid product Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 238000004064 recycling Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
- C07C409/04—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom being acyclic
- C07C409/08—Compounds containing six-membered aromatic rings
- C07C409/10—Cumene hydroperoxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C07C407/003—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Cumene hydroperoxide is prepared in a continuous process which comprises the following steps: (1) reacting cumene with oxygen at 80-120 in a zone to which there is supplied (a) fresh cumene of at least 99.8% purity and recycle cumene from step (3) and (b) an oxygen-containing gas containing at least 8% (mol.) of oxygen the amounts of (a) and (b) supplied being such that the ratio of the number of moles of oxygen supplied per hour to the " maximum number of moles of oxygen consumable " per hour is at least 0À25:1, the reaction conditions being such that the concentration of cumene hydroperoxide in the reaction zone is maintained at 8-40% (weight) and the exit gases contain 3-10% (weight) of oxygen, the reaction being carried out in the absence of initiator, catalyst and alkalizing agent (2) separating unreacted cumene from the hydroperoxide by vacuum flash distillation of the liquid product of step (1) and condensation of the exit gases from step (1), followed by separation of the cumene and (3) freeing the unreacted cumene from acid by treatment with an alkali metal hydroxide and recycling it to step (1). Preferably the process is carried out in a plurality of oxidation zones in which the temperature becomes successively lower in the range 80-120 C. The " maximum number of moles of oxygen consumable per hour " is defined as the number of moles of oxygen reacted per hour at the temperature under consideration when the feed gas is pure oxygen. The cumene hydroperoxide may be converted to phenol by known methods.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US84158569A | 1969-07-14 | 1969-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES378777A1 true ES378777A1 (en) | 1973-02-01 |
Family
ID=25285236
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES378777A Expired ES378777A1 (en) | 1969-07-14 | 1970-04-08 | Continuous method for the preparation of cumeno hydroperoxide. (Machine-translation by Google Translate, not legally binding) |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS549185B1 (en) |
DE (1) | DE2035496C3 (en) |
ES (1) | ES378777A1 (en) |
FR (1) | FR2050175A5 (en) |
GB (1) | GB1257595A (en) |
NL (1) | NL7008744A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5136740B2 (en) * | 1972-08-23 | 1976-10-12 |
-
1970
- 1970-04-08 ES ES378777A patent/ES378777A1/en not_active Expired
- 1970-06-03 GB GB1257595D patent/GB1257595A/en not_active Expired
- 1970-06-09 FR FR7021172A patent/FR2050175A5/fr not_active Expired
- 1970-06-15 NL NL7008744A patent/NL7008744A/xx unknown
- 1970-07-10 JP JP5997270A patent/JPS549185B1/ja active Pending
- 1970-07-17 DE DE19702035496 patent/DE2035496C3/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE2035496B2 (en) | 1980-02-28 |
FR2050175A5 (en) | 1971-03-26 |
GB1257595A (en) | 1971-12-22 |
DE2035496A1 (en) | 1972-01-20 |
JPS549185B1 (en) | 1979-04-21 |
DE2035496C3 (en) | 1980-10-16 |
NL7008744A (en) | 1971-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2582911A (en) | Preparation of acrylic esters | |
ES425528A1 (en) | Method for recovering a liquid-phase oxidation catalyst for preparation of terephthalic acid | |
US2632773A (en) | Manufacture of peroxidic compounds | |
GB1351033A (en) | Preparation of esters | |
US3907901A (en) | Continuous process for preparing cumene hydroperoxide | |
ES378777A1 (en) | Continuous method for the preparation of cumeno hydroperoxide. (Machine-translation by Google Translate, not legally binding) | |
US4350829A (en) | Process for preparing isobutyric acid | |
US2815373A (en) | Preparation of para-nitrobenzoic acid | |
US2681937A (en) | Process for the production of alkylaromatic hydroperoxides | |
ES434949A1 (en) | Process for producing ethylphenols | |
US2881220A (en) | Production of dimethyl phenyl carbinol | |
GB1017522A (en) | Improvements in or relating to the production of butyl acrylate | |
US2577768A (en) | Oxidation of cumene | |
US3862216A (en) | Process for preparing vinyl acetate | |
US3192256A (en) | Process for making peracids by the oxidation of aldehydes | |
GB1425751A (en) | Production of formaldehyde | |
US2465012A (en) | Manufacture of heptan-3:4-dione and ethyl propyl acrylic acid | |
US2769844A (en) | Process for preparation of para-alphacumyl phenol | |
Brill | Preparation of Hydroperoxide by the Autoxidation of 4-Vinylcyclohexane | |
US2450389A (en) | Manufacture of crotonic acid | |
SU445262A1 (en) | The method of obtaining cyclohexen-2-diol-1,4 | |
GB1494459A (en) | Process for preparation of diacetoxybutene | |
ES366991A1 (en) | Process for working-up crude liquid vinyl acetate | |
RU2146670C1 (en) | Cumene hydroperoxide production process | |
SU584756A3 (en) | Method of preparing ethylphenol |