JPS6348860B2 - - Google Patents
Info
- Publication number
- JPS6348860B2 JPS6348860B2 JP9690480A JP9690480A JPS6348860B2 JP S6348860 B2 JPS6348860 B2 JP S6348860B2 JP 9690480 A JP9690480 A JP 9690480A JP 9690480 A JP9690480 A JP 9690480A JP S6348860 B2 JPS6348860 B2 JP S6348860B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- chlorobenzene
- nitration
- acid
- sulfuric acid
- 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
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 36
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 33
- 238000006396 nitration reaction Methods 0.000 claims description 16
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 14
- 229910017604 nitric acid Inorganic materials 0.000 claims description 14
- BFCFYVKQTRLZHA-UHFFFAOYSA-N 1-chloro-2-nitrobenzene Chemical class [O-][N+](=O)C1=CC=CC=C1Cl BFCFYVKQTRLZHA-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 4
- 230000000802 nitrating effect Effects 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 23
- 238000000034 method Methods 0.000 description 19
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000007086 side reaction Methods 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- KMAQZIILEGKYQZ-UHFFFAOYSA-N 1-chloro-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(Cl)=C1 KMAQZIILEGKYQZ-UHFFFAOYSA-N 0.000 description 2
- CZGCEKJOLUNIFY-UHFFFAOYSA-N 4-Chloronitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C=C1 CZGCEKJOLUNIFY-UHFFFAOYSA-N 0.000 description 2
- VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- AWPVYCXXUJPMOG-UHFFFAOYSA-N [N+](=O)(O)[O-].[S] Chemical compound [N+](=O)(O)[O-].[S] AWPVYCXXUJPMOG-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002027 dichloromethane extract Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9690480A JPS5724331A (en) | 1980-07-17 | 1980-07-17 | Nitration of chlorobenzene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9690480A JPS5724331A (en) | 1980-07-17 | 1980-07-17 | Nitration of chlorobenzene |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5724331A JPS5724331A (en) | 1982-02-08 |
JPS6348860B2 true JPS6348860B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1988-09-30 |
Family
ID=14177350
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9690480A Granted JPS5724331A (en) | 1980-07-17 | 1980-07-17 | Nitration of chlorobenzene |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5724331A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1056829C (zh) * | 1995-10-20 | 2000-09-27 | 清华大学 | 催化硝化制备硝基氯苯的方法 |
-
1980
- 1980-07-17 JP JP9690480A patent/JPS5724331A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5724331A (en) | 1982-02-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110590557A (zh) | 一种芳基酚类或芳基醚类衍生物的硝化方法 | |
Mészáros et al. | Exploiting a silver–bismuth hybrid material as heterogeneous noble metal catalyst for decarboxylations and decarboxylative deuterations of carboxylic acids under batch and continuous flow conditions | |
US4178308A (en) | Process for the preparation of 1-amino-8-naphthol-3,6-disulphonic acid (H-acid) | |
US4109093A (en) | Process for making 2-(4'-aminophenyl) 5-amino benzimidazole | |
JPS6348860B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JPS598257B2 (ja) | 2−ニトロ−4,6−ジクロル−5−メチルフエノ−ルの製造方法 | |
CN108752218B (zh) | 一种度鲁特韦关键中间体2,4-二氟苄胺制备的路线 | |
EP0415595A1 (en) | Fluorobenzene derivatives | |
US4434304A (en) | Synthesis of trinitrophloroglucinol | |
JPH0149137B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JPH0524146B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
CN107903203B (zh) | 一种3,4-双硝基邻苯二甲酰亚胺的合成方法 | |
JP2003286230A (ja) | ニトロトルエンの製造方法 | |
CN108707077A (zh) | 以硝基甲苯为原料一步法制备tnt的方法 | |
JPH0419987B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US3719717A (en) | Process for the production of aromatic dinitrohalogen compounds | |
US3910995A (en) | Process for preparing 2,5-dihalo-3-nitrobenzoic acid | |
US4288620A (en) | Process for the production of 4-acylamido-2-nitro-1-alkoxybenzenes | |
CN117003644B (zh) | 一种合成2-氯-6-硝基甲苯的方法 | |
CN103936593B (zh) | 2,4,6-三硝基-1,3-二(2’,4’-二硝基苯乙烯基)苯、制备及其应用 | |
EP0415585A1 (en) | Fluorobenzene derivatives | |
JPH06329607A (ja) | イミノジコハク酸金属塩の製造方法 | |
SU938540A1 (ru) | Способ получени замещенных 4,8-диамино-1,5-диоксиантрахинона | |
US2311282A (en) | Nitrated bornyl phenols and the method of preparing the same | |
JPH04235956A (ja) | アントラニル酸の製造法 |