GB1243313A - Organic peroxides - Google Patents
Organic peroxidesInfo
- Publication number
- GB1243313A GB1243313A GB8229/70A GB822970A GB1243313A GB 1243313 A GB1243313 A GB 1243313A GB 8229/70 A GB8229/70 A GB 8229/70A GB 822970 A GB822970 A GB 822970A GB 1243313 A GB1243313 A GB 1243313A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aliphatic
- peroxides
- isopropyl
- joined
- aromatic radical
- 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
- 150000001451 organic peroxides Chemical class 0.000 title abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001336 alkenes Chemical class 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 2
- 150000002978 peroxides Chemical class 0.000 abstract 2
- OMRSFKWMIDIMKJ-UHFFFAOYSA-N 1h,3h-naphtho[1,8-cd]pyran Chemical compound C1=CC(COC2)=C3C2=CC=CC3=C1 OMRSFKWMIDIMKJ-UHFFFAOYSA-N 0.000 abstract 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- -1 t - butylperoxy Chemical group 0.000 abstract 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
-
- 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
- C07C409/00—Peroxy compounds
- C07C409/16—Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/16—Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides
- C07C409/18—Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides at least one of the carbon atoms belonging to a ring other than a six-membered aromatic ring
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,243,313. Organic peroxides. PENNWALT CORP. 20 Feb., 1970, No. 8229/70. Heading C2C. Organic peroxides are produced by reacting (1) an olefin of general formula in which y is 1, 2 or 3; R<SP>1</SP> is a mono-, di- or trivalent aromatic radical depending on the value of y; R<SP>2</SP> and R<SP>3</SP> are each H, or an aliphatic, cycloaliphatic or aromatic radical; R<SP>4</SP> is an aliphatic or aromatic radical; with the provisos that R<SP>2</SP> and R<SP>3</SP> may be joined together to form a cyclic group; R<SP>4</SP> and either R<SP>2</SP> or R<SP>3</SP> may be joined together to form a cyclic group; R<SP>4</SP> and R<SP>1</SP> may be joined to form a fused ring group; R<SP>2</SP> or R<SP>3</SP> may be joined to R<SP>1</SP> to form a fused ring group; and when R<SP>1</SP> carries substituents at least one ring carbon atom ortho to a is unsubstituted; with (2) a halide of formula in which X is I, Br, C1 or F; and (3) an organic hydroxperoxide of the general formula in which R<SP>5</SP> is an aliphatic or cycloaliphatic radical, the reaction being carried out under substantially anhydrous conditions, in the absence of free acid, the relative amounts of reactants (1) and (3) being such that the mole ratio of-OOH groups in the hydroperoxide to ethylenic double bonds in the olefin is from 1À 1:1 to 2: 1. Examples are given of the preparation of dicumyl peroxide; 1,4-bis[a-(t-butylperoxy) - isopropyl]benzene and 4 - [a - (t - butylperoxy) isopropyl] - α,α,α<SP>1</SP>,α<SP>1</SP>- tetramethyd naphthalan. This latter compound is preparelby reacting 1,2,4 tris (a-hydroxy isopropyl) benzene with hydrochloric acid to give 4-(achloroisopropyl) - a,a,a<SP>1</SP>,a1 - tetramethylnaphthalan which is reacted with t-butylhydroperoxide and 4 - isopropenyl - α,α,α<SP>1</SP>,α<SP>1</SP>- tetramethyl phthalan. A list of peroxides made by the process of the invention is also given and this includes peroxides carrying a chlorine or fluorine substituent.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8229/70A GB1243313A (en) | 1970-02-20 | 1970-02-20 | Organic peroxides |
| DE2016108A DE2016108C3 (en) | 1970-02-20 | 1970-04-03 | Process for the production of organic peroxides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8229/70A GB1243313A (en) | 1970-02-20 | 1970-02-20 | Organic peroxides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1243313A true GB1243313A (en) | 1971-08-18 |
Family
ID=9848442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8229/70A Expired GB1243313A (en) | 1970-02-20 | 1970-02-20 | Organic peroxides |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE2016108C3 (en) |
| GB (1) | GB1243313A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4159389A (en) * | 1978-05-16 | 1979-06-26 | Reichhold Chemicals, Inc. | Process for the production of dicumyl peroxide |
| US4243821A (en) * | 1979-09-13 | 1981-01-06 | Pennwalt Corporation | Process for the preparation of symmetrical dicumyl peroxides |
| US4374279A (en) * | 1980-12-02 | 1983-02-15 | Euteco Impianti S.P.A. | Process for the preparation of dicumyl peroxide |
| US4374280A (en) * | 1980-02-12 | 1983-02-15 | Euteco Impianti S.P.A. | Process for the preparation of dicumyl peroxide |
| CN103804264A (en) * | 2012-11-09 | 2014-05-21 | 中国石油化工集团公司 | Processing method of DCP (dicumyl peroxide) crystallization mother liquor |
| CN119874589A (en) * | 2025-03-27 | 2025-04-25 | 山东博远化工有限公司 | Dicumyl peroxide and preparation method and application thereof |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2916572A1 (en) * | 1979-04-24 | 1980-11-13 | Peroxid Chemie Gmbh | METHOD FOR THE DISTILLATIVE SEPARATION OF TERT.-ALKYL HYDROPEROXIDES AND DERTERT.-ALKYL PEROXIDES |
| DE3633308A1 (en) * | 1986-09-30 | 1988-03-31 | Peroxid Chemie Gmbh | METHOD FOR PRODUCING T-ALKYL-T-ARALKYL PEROXIDES |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3267066A (en) * | 1960-06-08 | 1966-08-16 | Konink Ind Mij Voorheen Noury | Process for the cross-linking of polyolefins and for the vulcanization of rubber |
| BE619409A (en) * | 1961-06-30 |
-
1970
- 1970-02-20 GB GB8229/70A patent/GB1243313A/en not_active Expired
- 1970-04-03 DE DE2016108A patent/DE2016108C3/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4159389A (en) * | 1978-05-16 | 1979-06-26 | Reichhold Chemicals, Inc. | Process for the production of dicumyl peroxide |
| US4243821A (en) * | 1979-09-13 | 1981-01-06 | Pennwalt Corporation | Process for the preparation of symmetrical dicumyl peroxides |
| US4374280A (en) * | 1980-02-12 | 1983-02-15 | Euteco Impianti S.P.A. | Process for the preparation of dicumyl peroxide |
| US4374279A (en) * | 1980-12-02 | 1983-02-15 | Euteco Impianti S.P.A. | Process for the preparation of dicumyl peroxide |
| CN103804264A (en) * | 2012-11-09 | 2014-05-21 | 中国石油化工集团公司 | Processing method of DCP (dicumyl peroxide) crystallization mother liquor |
| CN103804264B (en) * | 2012-11-09 | 2016-08-24 | 中国石油化工集团公司 | The method processing DCP crystalline mother solution |
| CN119874589A (en) * | 2025-03-27 | 2025-04-25 | 山东博远化工有限公司 | Dicumyl peroxide and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2016108C3 (en) | 1981-12-24 |
| DE2016108A1 (en) | 1971-10-21 |
| DE2016108B2 (en) | 1974-11-21 |
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