GB845036A - Derivatives of hexachlorotoluene - Google Patents
Derivatives of hexachlorotolueneInfo
- Publication number
- GB845036A GB845036A GB298/58A GB29858A GB845036A GB 845036 A GB845036 A GB 845036A GB 298/58 A GB298/58 A GB 298/58A GB 29858 A GB29858 A GB 29858A GB 845036 A GB845036 A GB 845036A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hexachlorotoluene
- hexachlorocyclopentadiene
- chloromethyl
- starting
- preparation
- 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
- GXEUUGWYEFEZQH-UHFFFAOYSA-N 1,2,3-trichloro-4-(trichloromethyl)benzene Chemical class ClC1=CC=C(C(Cl)(Cl)Cl)C(Cl)=C1Cl GXEUUGWYEFEZQH-UHFFFAOYSA-N 0.000 title abstract 3
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 abstract 6
- 238000002360 preparation method Methods 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 3
- -1 (1-hydroxy, 1-methylpropyl) hexachloro-toluene cyclopentyl-hexachlorotoluene Chemical compound 0.000 abstract 2
- BEHHMGYFOAIYHQ-UHFFFAOYSA-N 1,2,3-trichloro-4,5-bis(chloromethyl)-6-(trichloromethyl)benzene Chemical compound ClCC1=C(C(=C(C(=C1C(Cl)(Cl)Cl)Cl)Cl)Cl)CCl BEHHMGYFOAIYHQ-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000749 insecticidal effect Effects 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- IHAXIFZOERJWDF-UHFFFAOYSA-N 1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hepta-2,5-diene Chemical class C1=CC2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl IHAXIFZOERJWDF-UHFFFAOYSA-N 0.000 abstract 1
- HSPNRCOLHMQAIK-UHFFFAOYSA-N 1,2,3-trichloro-4-(2,3,4-trichlorocyclohepta-1,3-dien-1-yl)cyclohepta-1,3-diene Chemical compound ClC1=C(C(=C(CCC1)C1=C(C(=C(CCC1)Cl)Cl)Cl)Cl)Cl HSPNRCOLHMQAIK-UHFFFAOYSA-N 0.000 abstract 1
- RCHDLEVSZBOHOS-UHFFFAOYSA-N 1,4-dichlorobut-2-yne Chemical compound ClCC#CCCl RCHDLEVSZBOHOS-UHFFFAOYSA-N 0.000 abstract 1
- QZVGTTNYDBYLPI-UHFFFAOYSA-N 1-bromo-3,4,5-trichloro-2-methyl-6-(trichloromethyl)benzene Chemical compound BrC1=C(C(=C(C(=C1C(Cl)(Cl)Cl)Cl)Cl)Cl)C QZVGTTNYDBYLPI-UHFFFAOYSA-N 0.000 abstract 1
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 abstract 1
- UBNWNTSMJFYRDZ-UHFFFAOYSA-N 2,3,4-trichloro-1-phenyl-5-(trichloromethyl)benzene Chemical compound C1(=CC=CC=C1)C=1C(=C(C(=C(C(Cl)(Cl)Cl)C=1)Cl)Cl)Cl UBNWNTSMJFYRDZ-UHFFFAOYSA-N 0.000 abstract 1
- ZEHIHRPSBKRNLY-UHFFFAOYSA-N 2,3,4-trichloro-5-(chloromethyl)benzoic acid Chemical compound ClCC=1C(=C(C(=C(C(=O)O)C1)Cl)Cl)Cl ZEHIHRPSBKRNLY-UHFFFAOYSA-N 0.000 abstract 1
- SSUFZHQZQHWRPK-UHFFFAOYSA-N 3,4,5-trichloro-6-(trichloromethyl)phthalic acid Chemical compound C(=O)(O)C1=C(C(=C(C(=C1C(Cl)(Cl)Cl)Cl)Cl)Cl)C(=O)O SSUFZHQZQHWRPK-UHFFFAOYSA-N 0.000 abstract 1
- RQWAJGPYXWVGKW-UHFFFAOYSA-N 3-[2,3,4-trichloro-5-(trichloromethyl)phenyl]benzene-1,2-diamine Chemical compound NC=1C(=C(C=CC=1)C=1C(=C(C(=C(C(Cl)(Cl)Cl)C=1)Cl)Cl)Cl)N RQWAJGPYXWVGKW-UHFFFAOYSA-N 0.000 abstract 1
- TVUGJNJMVHGXRT-UHFFFAOYSA-N 3-[2,3,4-trichloro-5-(trichloromethyl)phenyl]propanoic acid Chemical compound C(=O)(O)CCC=1C(=C(C(=C(C(Cl)(Cl)Cl)C=1)Cl)Cl)Cl TVUGJNJMVHGXRT-UHFFFAOYSA-N 0.000 abstract 1
- 241000253994 Acyrthosiphon pisum Species 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 241000462639 Epilachna varivestis Species 0.000 abstract 1
- 241000305186 Persectania ewingii Species 0.000 abstract 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 1
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- SOHIUKGQJAOUFZ-UHFFFAOYSA-N [3,4,5-trichloro-2-(hydroxymethyl)-6-(trichloromethyl)phenyl]methanol Chemical compound OCC1=C(C(=C(C(=C1C(Cl)(Cl)Cl)Cl)Cl)Cl)CO SOHIUKGQJAOUFZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000012043 crude product Substances 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- FMVJYQGSRWVMQV-UHFFFAOYSA-N ethyl propiolate Chemical compound CCOC(=O)C#C FMVJYQGSRWVMQV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 229910000286 fullers earth Inorganic materials 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 abstract 1
- LJZPPWWHKPGCHS-UHFFFAOYSA-N propargyl chloride Chemical compound ClCC#C LJZPPWWHKPGCHS-UHFFFAOYSA-N 0.000 abstract 1
- 230000008707 rearrangement Effects 0.000 abstract 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/30—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by a Diels-Alder synthesis
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/06—Nitrogen directly attached to an aromatic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/358—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by isomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/02—Monocyclic aromatic halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/68—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
- C07C67/293—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
- C08K5/03—Halogenated hydrocarbons aromatic, e.g. C6H5-CH2-Cl
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/44—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing eight carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US632986A US2946817A (en) | 1957-01-08 | 1957-01-08 | Ring-substituted derivatives of alpha, alpha, alpha-2, 3, 4-hexachlorotoluene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB845036A true GB845036A (en) | 1960-08-17 |
Family
ID=24537821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB298/58A Expired GB845036A (en) | 1957-01-08 | 1958-01-03 | Derivatives of hexachlorotoluene |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2946817A (cg-RX-API-DMAC10.html) |
| DE (1) | DE1418455A1 (cg-RX-API-DMAC10.html) |
| GB (1) | GB845036A (cg-RX-API-DMAC10.html) |
| NL (2) | NL223867A (cg-RX-API-DMAC10.html) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3088977A (en) * | 1959-05-18 | 1963-05-07 | Velsicol Chemical Corp | Hexachlorotetrahydromethanoindene amine compounds |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1878463A (en) * | 1929-04-06 | 1932-09-20 | Dow Chemical Co | Method of making halogenated benzoic acid derivatives |
| US2132361A (en) * | 1934-12-05 | 1938-10-04 | Ig Farbenindustrie Ag | Process of chlorinating methylaromatic compounds |
| US2695873A (en) * | 1952-04-04 | 1954-11-30 | Hooker Electrochemical Co | Process for chlorinating methyl aromatic compounds |
| NL82876C (cg-RX-API-DMAC10.html) * | 1954-01-12 | |||
| CH324672A (de) * | 1954-07-08 | 1957-10-15 | Ciba Geigy | Verfahren zur Herstellung von Trichlormethyl-halogenbenzolen |
-
0
- NL NL111158D patent/NL111158C/xx active
- NL NL223867D patent/NL223867A/xx unknown
-
1957
- 1957-01-08 US US632986A patent/US2946817A/en not_active Expired - Lifetime
-
1958
- 1958-01-03 GB GB298/58A patent/GB845036A/en not_active Expired
- 1958-01-08 DE DE19581418455 patent/DE1418455A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NL111158C (cg-RX-API-DMAC10.html) | |
| DE1418455A1 (de) | 1968-11-07 |
| NL223867A (cg-RX-API-DMAC10.html) | |
| US2946817A (en) | 1960-07-26 |
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