SU193473A1 - - Google Patents
Info
- Publication number
- SU193473A1 SU193473A1 SU948996A SU948996A SU193473A1 SU 193473 A1 SU193473 A1 SU 193473A1 SU 948996 A SU948996 A SU 948996A SU 948996 A SU948996 A SU 948996A SU 193473 A1 SU193473 A1 SU 193473A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- chloride
- sulfuric acid
- yield
- ether
- dichlorobenzene
- Prior art date
Links
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 14
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 8
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 150000001555 benzenes Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OMZINLIPPVNUOG-UHFFFAOYSA-N 1,4-dichloro-2-(chloromethyl)benzene Chemical compound ClCC1=CC(Cl)=CC=C1Cl OMZINLIPPVNUOG-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001804 chlorine Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- UBJKMVAYDQUJSJ-UHFFFAOYSA-N 1,2,4-trichloro-5-(chloromethyl)benzene Chemical compound ClCC1=CC(Cl)=C(Cl)C=C1Cl UBJKMVAYDQUJSJ-UHFFFAOYSA-N 0.000 description 1
- AIPJZPPOFWCJRC-UHFFFAOYSA-N 1,2-dichloro-3-(chloromethyl)benzene Chemical compound ClCC1=CC=CC(Cl)=C1Cl AIPJZPPOFWCJRC-UHFFFAOYSA-N 0.000 description 1
- YZIFVWOCPGPNHB-UHFFFAOYSA-N 1,2-dichloro-4-(chloromethyl)benzene Chemical compound ClCC1=CC=C(Cl)C(Cl)=C1 YZIFVWOCPGPNHB-UHFFFAOYSA-N 0.000 description 1
- MBAWENWZCTWAPT-UHFFFAOYSA-N 1,4-dichloro-2,5-bis(chloromethyl)benzene Chemical compound ClCC1=CC(Cl)=C(CCl)C=C1Cl MBAWENWZCTWAPT-UHFFFAOYSA-N 0.000 description 1
- AUAXYMOBWXOEQD-UHFFFAOYSA-N 2,5-dichloro-3-nitrobenzoic acid Chemical compound OC(=O)C1=CC(Cl)=CC([N+]([O-])=O)=C1Cl AUAXYMOBWXOEQD-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU193473A1 true SU193473A1 (fr) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0034402B1 (fr) | Procédé de préparation de dérivés d'éthers diphényliques fluorosubstitués et benzènes halogénés fluorosubstitués à utiliser dans ce procédé | |
| US4582948A (en) | 3-chloro-4-fluoro-5-nitrobenzotrifluoride | |
| DK155084B (da) | Fremgangsmaade til fremstilling af meta-aryloxy-benzaldehyder | |
| US3954817A (en) | Process for the manufacture of perfluoroalkylmethylene-carboxylic acids | |
| CA1051032A (fr) | Synthese de nitrobenzaldehyde-2 et intermediaires | |
| SU606547A3 (ru) | Способ получени трифторметилбензолов | |
| US5478963A (en) | 2,3-difluoro-6-nitrobenzonitrile and 2-chloro-5,6-difluorobenzonitrile-(2,3-difluoro-6-chlorobenzonitrile), process for their preparation and their use for the preparation of 2,3,6-trifluorobenzoic acid | |
| JPS6312048B2 (fr) | ||
| JPH0912508A (ja) | 2−フルオロ−イソ酪酸アルキルの製造方法 | |
| US3703546A (en) | Preparation of 3-amino-2,5-dichlorobenzoic acid | |
| RU2850233C1 (ru) | Способ получения октафторциклопентена | |
| JPH06228051A (ja) | ハロゲン化安息香酸の製造方法 | |
| US4876404A (en) | Preparation of dichlorotrifluoromethyltoluenes including novel isomers | |
| FR2602766A1 (fr) | Composes dichlorotrifluoromethylnitrotoluenes et procede de preparation d'aminotrifluoromethyltoluenes a partir de ces composes | |
| SU205703A1 (ru) | Способ получения 2,3,6-трихлорбензойной кислоты | |
| US4704483A (en) | 3,4-difluoro-5-nitrobenzotrifluoride and preparation of fluoro-nitro-benzotrifluorides | |
| SU183767A1 (ru) | Способ получения ацетилнитробензоилперекиси | |
| SU192777A1 (ru) | Способ получения 4-4'-дихлордибутилового эфира | |
| US4603222A (en) | Method for the preparation of nitrodiphenyl ethers | |
| SU167494A1 (ru) | Способ получения парадитретичноамилбензола | |
| JP3261474B2 (ja) | 2−クロロ−4,5−ジフルオロ安息香酸の製造法 | |
| SU281481A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ л-ФЕНОКСИФЕНОЛА | |
| IL106166A (en) | Process for the production and production of alonitroalkanes | |
| SU176883A1 (ru) | Способ получения 3-нитро-2,5-дихлорбензойиойкислоты | |
| SU1004346A1 (ru) | Способ получени монохлоруксусной кислоты |