GB1317497A - Aqueous acid phase nitration of 4-substituted anilines - Google Patents
Aqueous acid phase nitration of 4-substituted anilinesInfo
- Publication number
- GB1317497A GB1317497A GB2209071A GB2209071A GB1317497A GB 1317497 A GB1317497 A GB 1317497A GB 2209071 A GB2209071 A GB 2209071A GB 2209071 A GB2209071 A GB 2209071A GB 1317497 A GB1317497 A GB 1317497A
- Authority
- GB
- United Kingdom
- Prior art keywords
- toluidine
- reaction
- bis
- derivative
- aromatic amine
- 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
- -1 4-substituted anilines Chemical class 0.000 title abstract 2
- 238000006396 nitration reaction Methods 0.000 title abstract 2
- 239000011260 aqueous acid Substances 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 150000002500 ions Chemical class 0.000 abstract 2
- GDPRJMAJFSDBKX-UHFFFAOYSA-N n,n-bis(2-chloroethyl)-4-methylaniline Chemical compound CC1=CC=C(N(CCCl)CCCl)C=C1 GDPRJMAJFSDBKX-UHFFFAOYSA-N 0.000 abstract 2
- 150000003513 tertiary aromatic amines Chemical class 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- JUVSRZCUMWZBFK-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-methylanilino]ethanol Chemical compound CC1=CC=C(N(CCO)CCO)C=C1 JUVSRZCUMWZBFK-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000006267 biphenyl group Chemical group 0.000 abstract 1
- 238000005660 chlorination reaction Methods 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- PMZYCDUCCVXQFE-UHFFFAOYSA-N n,n-bis(2-chloroethyl)-4-methyl-2-nitroaniline Chemical compound CC1=CC=C(N(CCCl)CCCl)C([N+]([O-])=O)=C1 PMZYCDUCCVXQFE-UHFFFAOYSA-N 0.000 abstract 1
- 229910017604 nitric acid Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000004992 toluidines Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B43/00—Formation or introduction of functional groups containing nitrogen
- C07B43/02—Formation or introduction of functional groups containing nitrogen of nitro or nitroso groups
-
- 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
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (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 |
|---|---|---|---|
| US2010770A | 1970-03-16 | 1970-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1317497A true GB1317497A (en) | 1973-05-16 |
Family
ID=21796788
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2209071A Expired GB1317497A (en) | 1970-03-16 | 1971-04-19 | Aqueous acid phase nitration of 4-substituted anilines |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3726922A (enExample) |
| BE (1) | BE762228A (enExample) |
| CA (1) | CA995689A (enExample) |
| DE (1) | DE2111863A1 (enExample) |
| FR (1) | FR2083300B1 (enExample) |
| GB (1) | GB1317497A (enExample) |
| LU (1) | LU62587A1 (enExample) |
| NL (1) | NL7102775A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3442757A1 (de) * | 1984-11-23 | 1986-05-28 | Wella Ag, 6100 Darmstadt | Verwendung von 2-nitroanilinderivaten in haarfaerbemitteln und neue 2-nitroanilinderivate |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE571267A (enExample) * | 1957-09-17 | |||
| US3442639A (en) * | 1965-12-22 | 1969-05-06 | Lilly Co Eli | Process of selectively eliminating weeds |
-
1970
- 1970-03-16 US US00020107A patent/US3726922A/en not_active Expired - Lifetime
-
1971
- 1971-01-19 CA CA103,050A patent/CA995689A/en not_active Expired
- 1971-01-29 BE BE762228A patent/BE762228A/xx unknown
- 1971-02-11 FR FR717104617A patent/FR2083300B1/fr not_active Expired
- 1971-02-12 LU LU62587D patent/LU62587A1/xx unknown
- 1971-03-02 NL NL7102775A patent/NL7102775A/xx unknown
- 1971-03-12 DE DE19712111863 patent/DE2111863A1/de active Pending
- 1971-04-19 GB GB2209071A patent/GB1317497A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL7102775A (enExample) | 1971-09-20 |
| FR2083300A1 (enExample) | 1971-12-17 |
| US3726922A (en) | 1973-04-10 |
| LU62587A1 (enExample) | 1971-08-19 |
| BE762228A (fr) | 1971-07-01 |
| CA995689A (en) | 1976-08-24 |
| FR2083300B1 (enExample) | 1973-06-08 |
| DE2111863A1 (de) | 1971-10-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |