GB941803A - Improvements in or relating to diazotype copying processes - Google Patents
Improvements in or relating to diazotype copying processesInfo
- Publication number
- GB941803A GB941803A GB3415660A GB3415660A GB941803A GB 941803 A GB941803 A GB 941803A GB 3415660 A GB3415660 A GB 3415660A GB 3415660 A GB3415660 A GB 3415660A GB 941803 A GB941803 A GB 941803A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- dimethyl
- morpholino
- phenol
- dialkyl
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- LQMMFVPUIVBYII-UHFFFAOYSA-N 2-methylmorpholine Chemical compound CC1CNCCO1 LQMMFVPUIVBYII-UHFFFAOYSA-N 0.000 abstract 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000006149 azo coupling reaction Methods 0.000 abstract 1
- 150000001555 benzenes Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000003840 hydrochlorides Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Abstract
Hydroxy - dialkyl-morpholinomethyl-benzenes, other than the 2,5 dialkyl compound of the parent Specification are used as azo-coupling components in photographic materials (see Division G2). The alkyl substituents in the benzene nucleus contain not more than 5 carbon atoms and may be straight or branched chain. The morpholine residue may also contain alkyl substituents. A long list of such compounds, including the free phenols and their hydrochlorides, is given and the following are used in specific examples:-(1) 2,5-dimethyl-4-[21,51 -dimethyl - morpholino - (41) - methyl] - phenol hydrochloride; (2) 2,5-dimethyl-4-[21 -methyl-morpholino-(41)-methyl]-phenol hydrochloride; (3) 2,5,-dimethyl-4-[21-ethyl-morpholino - (41) -methyl]-phenol hydrochloride; and (4) (a) 3,5-dimethyl-2-[morpholino-(41)-methyl]-phenol and (b) the corresponding 21-methyl-morpholino compound. The preparation of compounds (2) and (4b) is described, the reactants being the appropriate dialkyl phenol, 2-methyl morpholine and 30% aqueous formaldehyde.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEK38880A DE1134886B (en) | 1959-10-10 | 1959-10-10 | Diazotype copy layers, especially for the production of intermediate originals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB941803A true GB941803A (en) | 1963-11-13 |
Family
ID=7221536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3415660A Expired GB941803A (en) | 1959-10-10 | 1960-10-05 | Improvements in or relating to diazotype copying processes |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE595814A (en) |
| CA (1) | CA685078A (en) |
| CH (1) | CH393083A (en) |
| DE (1) | DE1134886B (en) |
| DK (1) | DK114744B (en) |
| GB (1) | GB941803A (en) |
| NL (2) | NL103449C (en) |
-
0
- BE BE595814D patent/BE595814A/xx unknown
- CA CA685078A patent/CA685078A/en not_active Expired
- NL NL256696D patent/NL256696A/xx unknown
- NL NL103449D patent/NL103449C/xx active
-
1959
- 1959-10-10 DE DEK38880A patent/DE1134886B/en active Pending
-
1960
- 1960-10-05 GB GB3415660A patent/GB941803A/en not_active Expired
- 1960-10-07 CH CH1129460A patent/CH393083A/en unknown
- 1960-10-10 DK DK397060A patent/DK114744B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK114744B (en) | 1969-07-28 |
| CH393083A (en) | 1965-05-31 |
| CA685078A (en) | 1964-04-21 |
| DE1134886B (en) | 1962-08-16 |
| NL103449C (en) | |
| NL256696A (en) | |
| BE595814A (en) |
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