GB949574A - Improvements in or relating to benzene dicarboxylic acid chlorides - Google Patents
Improvements in or relating to benzene dicarboxylic acid chloridesInfo
- Publication number
- GB949574A GB949574A GB3367960A GB3367960A GB949574A GB 949574 A GB949574 A GB 949574A GB 3367960 A GB3367960 A GB 3367960A GB 3367960 A GB3367960 A GB 3367960A GB 949574 A GB949574 A GB 949574A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- hexachloro
- xylene
- chloride
- chlorides
- 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
- FYXKZNLBZKRYSS-UHFFFAOYSA-N benzene-1,2-dicarbonyl chloride Chemical class ClC(=O)C1=CC=CC=C1C(Cl)=O FYXKZNLBZKRYSS-UHFFFAOYSA-N 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 5
- -1 isophthaloyl Chemical group 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 5
- OTEKOJQFKOIXMU-UHFFFAOYSA-N 1,4-bis(trichloromethyl)benzene Chemical group ClC(Cl)(Cl)C1=CC=C(C(Cl)(Cl)Cl)C=C1 OTEKOJQFKOIXMU-UHFFFAOYSA-N 0.000 abstract 4
- 150000001805 chlorine compounds Chemical class 0.000 abstract 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 2
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 235000013312 flour Nutrition 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 230000001069 nematicidal effect Effects 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 2
- 229920000570 polyether Polymers 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- LJMNEQZBOODJQR-UHFFFAOYSA-N 2-(trichloromethyl)benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1C(Cl)(Cl)Cl LJMNEQZBOODJQR-UHFFFAOYSA-N 0.000 abstract 1
- 240000005020 Acaciella glauca Species 0.000 abstract 1
- 241000251468 Actinopterygii Species 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- 244000299507 Gossypium hirsutum Species 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 241001002197 Juglans mollis Species 0.000 abstract 1
- 239000005909 Kieselgur Substances 0.000 abstract 1
- 241000244206 Nematoda Species 0.000 abstract 1
- 241000244199 Panagrellus redivivus Species 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 241000221577 Uromyces appendiculatus Species 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 238000000338 in vitro Methods 0.000 abstract 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical class Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 abstract 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000008188 pellet Substances 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- 150000003022 phthalic acids Chemical class 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 235000003499 redwood Nutrition 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US84395359A | 1959-10-02 | 1959-10-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB949574A true GB949574A (en) | 1964-02-12 |
Family
ID=25291408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3367960A Expired GB949574A (en) | 1959-10-02 | 1960-09-30 | Improvements in or relating to benzene dicarboxylic acid chlorides |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE1170928B (enrdf_load_stackoverflow) |
| GB (1) | GB949574A (enrdf_load_stackoverflow) |
| NL (1) | NL256448A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3045440A4 (en) * | 2013-09-13 | 2017-03-01 | Shanghai Fanglun New Material Technology Co. Ltd. | Method for the preparation of trichloromethyl-group-substituted benzene |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR820698A (fr) * | 1936-04-17 | 1937-11-16 | Ig Farbenindustrie Ag | Procédé de préparation de chlorures d'acides polycarboxyliques appartenant à la série benzénique |
-
0
- NL NL256448D patent/NL256448A/xx unknown
- DE DED34414A patent/DE1170928B/de active Pending
-
1960
- 1960-09-30 GB GB3367960A patent/GB949574A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3045440A4 (en) * | 2013-09-13 | 2017-03-01 | Shanghai Fanglun New Material Technology Co. Ltd. | Method for the preparation of trichloromethyl-group-substituted benzene |
| RU2670436C2 (ru) * | 2013-09-13 | 2018-10-23 | Файнингс Ко. Лтд | Способ получения трихлорметилзамещенного бензола |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1170928B (de) | 1964-05-27 |
| NL256448A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB949574A (en) | Improvements in or relating to benzene dicarboxylic acid chlorides | |
| GB791875A (en) | Process for the preparation of per-fatty acids | |
| US3919301A (en) | Perfluoroalkyl sulphinic acids and a process for their production | |
| US2939872A (en) | Ethyl 3-(2, 4-dichlorophenyl) glycidate | |
| GB863550A (en) | 3-mercapto-phenthiazines | |
| US3360432A (en) | Chlorophenylcyclopropanecar-boxamide mite ovicides | |
| US3867448A (en) | Trifluoromethylphenyl-formamadines and acetamidines | |
| US3651224A (en) | Pesticidal pyrimidine derivative | |
| US2910477A (en) | Preparation of piperazine | |
| US3423416A (en) | Novel aromatic n-heterocyclic esters of diarylcarbamoyl or diarylthiocarbamoyl halides | |
| EP0002077B1 (en) | Esters of substituted cyclopropanecarboxylic acids and process for the preparation thereof | |
| US2931803A (en) | Fluorocarbon metalloid compounds of tetrafluoroethylene and sulfur, selenium or phosphorus and their preparation | |
| US2938919A (en) | Thiophosphoric acid esters and a process for their manufacture | |
| US3201444A (en) | Omicron-alkyl-omicron-cycloalkyl thiophosphoric acid s-phenylesters | |
| US3869509A (en) | N-alkyl-N(trihalomethylthio)-sulfamic acid chloride | |
| US2665202A (en) | Organic thiocyanate herbicides | |
| US3251884A (en) | Bis(haloalkyl)disulfides | |
| US2429391A (en) | Bis (carboxy methyl propyl) sulfide | |
| GB1244910A (en) | Preparation of (cis-1,2-epoxypropyl)phosphonic acid, derivatives thereof and intermediates therefor | |
| US3983131A (en) | Process for the production of 1,1'-peroxydicyclohexylamine | |
| US3546287A (en) | Synthesis of 1,2,3,4 - tetrahydro - 5 - naphthalene sulfonylfluoride (1) and 1,2,3,4-tetrahydro - 6 - naphthalene sulfonylfluoride | |
| US2654760A (en) | Preparation of 4-methyl-5-(beta-hydroxyethyl)-thiazole | |
| US2994715A (en) | Preparation of methyloxyfluorophosphine | |
| US3251850A (en) | Certain fluoro-dichloromethyldithiobenzazole compounds | |
| US3218336A (en) | 2, 5-dihydrothiophene s-substituted salts and process therefor |