GB1246254A - Diazonium compounds and their use in diazotype processes - Google Patents
Diazonium compounds and their use in diazotype processesInfo
- Publication number
- GB1246254A GB1246254A GB275470A GB275470A GB1246254A GB 1246254 A GB1246254 A GB 1246254A GB 275470 A GB275470 A GB 275470A GB 275470 A GB275470 A GB 275470A GB 1246254 A GB1246254 A GB 1246254A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- nitrobenzene
- give
- chloro
- compound
- 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
- 150000001989 diazonium salts Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 13
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- YQNUXMCUBCQQAK-UHFFFAOYSA-N n,n-dimethyl-4-nitro-2-phenylaniline Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=C1C1=CC=CC=C1 YQNUXMCUBCQQAK-UHFFFAOYSA-N 0.000 abstract 2
- 230000000802 nitrating effect Effects 0.000 abstract 2
- FIQBDKFALPAHOK-UHFFFAOYSA-N 1-chloro-2-nitro-4-phenylbenzene Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(C=2C=CC=CC=2)=C1 FIQBDKFALPAHOK-UHFFFAOYSA-N 0.000 abstract 1
- POLMDYPZWBMABD-UHFFFAOYSA-N 1-chloro-4-nitro-2-phenylbenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C(C=2C=CC=CC=2)=C1 POLMDYPZWBMABD-UHFFFAOYSA-N 0.000 abstract 1
- YOJKKXRJMXIKSR-UHFFFAOYSA-N 1-nitro-2-phenylbenzene Chemical group [O-][N+](=O)C1=CC=CC=C1C1=CC=CC=C1 YOJKKXRJMXIKSR-UHFFFAOYSA-N 0.000 abstract 1
- TWBPWBPGNQWFSJ-UHFFFAOYSA-N 2-phenylaniline Chemical group NC1=CC=CC=C1C1=CC=CC=C1 TWBPWBPGNQWFSJ-UHFFFAOYSA-N 0.000 abstract 1
- LFOCMKLBBPUNHA-UHFFFAOYSA-N 4-chloro-2-nitro-1-phenylbenzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC=C1C1=CC=CC=C1 LFOCMKLBBPUNHA-UHFFFAOYSA-N 0.000 abstract 1
- PBGKNXWGYQPUJK-UHFFFAOYSA-N 4-chloro-2-nitroaniline Chemical compound NC1=CC=C(Cl)C=C1[N+]([O-])=O PBGKNXWGYQPUJK-UHFFFAOYSA-N 0.000 abstract 1
- KCZGUJJXVDZLRG-UHFFFAOYSA-N 4-chloro-N,N-dimethyl-6-nitro-1-phenyldiazenylcyclohexa-2,4-dien-1-amine Chemical compound ClC1=CC(C(C=C1)(N=NC1=CC=CC=C1)N(C)C)[N+](=O)[O-] KCZGUJJXVDZLRG-UHFFFAOYSA-N 0.000 abstract 1
- HGCXDANGMCAFHL-UHFFFAOYSA-N 4-methyl-n-(4-nitro-2-phenylphenyl)benzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C([N+]([O-])=O)C=C1C1=CC=CC=C1 HGCXDANGMCAFHL-UHFFFAOYSA-N 0.000 abstract 1
- WFBXYWYRLONTJK-UHFFFAOYSA-N 4-nitro-2-phenylaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C1=CC=CC=C1 WFBXYWYRLONTJK-UHFFFAOYSA-N 0.000 abstract 1
- IBGNKLJXZBMJTN-UHFFFAOYSA-N 5-chloro-2-phenylaniline Chemical compound NC1=CC(Cl)=CC=C1C1=CC=CC=C1 IBGNKLJXZBMJTN-UHFFFAOYSA-N 0.000 abstract 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 abstract 1
- XEODAMARPBGSNM-UHFFFAOYSA-N N-(5-chloro-4-nitro-2-phenylphenyl)-4-methylbenzenesulfonamide Chemical compound S(=O)(=O)(C1=CC=C(C)C=C1)NC1=CC(=C(C=C1C1=CC=CC=C1)[N+](=O)[O-])Cl XEODAMARPBGSNM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 125000004659 aryl alkyl thio group Chemical group 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 abstract 1
- 229940045803 cuprous chloride Drugs 0.000 abstract 1
- 239000012954 diazonium Substances 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 abstract 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/54—Diazonium salts or diazo anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/07—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
- C07C205/11—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
- C07C205/12—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings the six-membered aromatic ring or a condensed ring system containing that ring being substituted by halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL6901305A NL6901305A (enrdf_load_stackoverflow) | 1969-01-27 | 1969-01-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1246254A true GB1246254A (en) | 1971-09-15 |
Family
ID=19805991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB275470A Expired GB1246254A (en) | 1969-01-27 | 1970-01-20 | Diazonium compounds and their use in diazotype processes |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE2003508A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2029455B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1246254A (enrdf_load_stackoverflow) |
| NL (1) | NL6901305A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011256158A (ja) * | 2010-05-12 | 2011-12-22 | Tosoh Corp | ビアリール化合物およびその製造方法、ならびにそのビアリール化合物を使用するカルバゾール誘導体の製造方法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2618429A1 (fr) * | 1987-07-24 | 1989-01-27 | Centre Nat Rech Scient | Nouveaux reactifs bifonctionnels photoactivables, leur preparation et leur application |
-
1969
- 1969-01-27 NL NL6901305A patent/NL6901305A/xx unknown
-
1970
- 1970-01-20 GB GB275470A patent/GB1246254A/en not_active Expired
- 1970-01-23 FR FR7002431A patent/FR2029455B1/fr not_active Expired
- 1970-01-27 DE DE19702003508 patent/DE2003508A1/de active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011256158A (ja) * | 2010-05-12 | 2011-12-22 | Tosoh Corp | ビアリール化合物およびその製造方法、ならびにそのビアリール化合物を使用するカルバゾール誘導体の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2003508A1 (de) | 1970-07-30 |
| FR2029455A1 (enrdf_load_stackoverflow) | 1970-10-23 |
| FR2029455B1 (enrdf_load_stackoverflow) | 1973-03-16 |
| NL6901305A (enrdf_load_stackoverflow) | 1970-07-29 |
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