ES209289A1 - UN PROCEDIMIENTO PARA LA OBTENCIoN DE NUEVOS DERIVADOS DE OXAZOLINA - Google Patents
UN PROCEDIMIENTO PARA LA OBTENCIoN DE NUEVOS DERIVADOS DE OXAZOLINAInfo
- Publication number
- ES209289A1 ES209289A1 ES0209289A ES209289A ES209289A1 ES 209289 A1 ES209289 A1 ES 209289A1 ES 0209289 A ES0209289 A ES 0209289A ES 209289 A ES209289 A ES 209289A ES 209289 A1 ES209289 A1 ES 209289A1
- Authority
- ES
- Spain
- Prior art keywords
- oxazoline
- hydroxyphenyl
- formula
- dichloro
- substituted
- 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
- 125000003504 2-oxazolinyl group Chemical class O1C(=NCC1)* 0.000 title 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 abstract 8
- 150000002918 oxazolines Chemical class 0.000 abstract 7
- -1 alkyl radicals Chemical class 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 239000000843 powder Substances 0.000 abstract 4
- ZMESHQOXZMOOQQ-UHFFFAOYSA-N 1-(naphthalen-1-ylmethyl)naphthalene Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZMESHQOXZMOOQQ-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 159000000000 sodium salts Chemical class 0.000 abstract 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229960000541 cetyl alcohol Drugs 0.000 abstract 2
- 239000007859 condensation product Substances 0.000 abstract 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 abstract 2
- 239000002270 dispersing agent Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 238000002156 mixing Methods 0.000 abstract 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- 238000009736 wetting Methods 0.000 abstract 2
- ZTFYJIXFKGPCHV-UHFFFAOYSA-N 2-propan-2-ylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C(C)C)=CC=C21 ZTFYJIXFKGPCHV-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000012024 dehydrating agents Substances 0.000 abstract 1
- 125000003963 dichloro group Chemical group Cl* 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 238000000227 grinding Methods 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 230000002140 halogenating effect Effects 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 abstract 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000012265 solid product Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/22—Luminous paints
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D263/14—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1241452A GB730192A (en) | 1952-05-16 | 1952-05-16 | New oxazoline derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES209289A1 true ES209289A1 (es) | 1954-06-16 |
Family
ID=10004161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0209289A Expired ES209289A1 (es) | 1952-05-16 | 1953-05-13 | UN PROCEDIMIENTO PARA LA OBTENCIoN DE NUEVOS DERIVADOS DE OXAZOLINA |
Country Status (8)
| Country | Link |
|---|---|
| BE (1) | BE520018A (enrdf_load_stackoverflow) |
| CH (1) | CH321108A (enrdf_load_stackoverflow) |
| DE (1) | DE1000819C2 (enrdf_load_stackoverflow) |
| DK (2) | DK80450C (enrdf_load_stackoverflow) |
| ES (1) | ES209289A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1079351A (enrdf_load_stackoverflow) |
| GB (1) | GB730192A (enrdf_load_stackoverflow) |
| NL (1) | NL88380C (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL275086A (enrdf_load_stackoverflow) * | 1961-02-22 | |||
| DE3411868A1 (de) * | 1984-03-30 | 1985-10-10 | The Dow Chemical Co., Midland, Mich. | Herstellung in fluessiger phase von 2-h-2-oxazolinen und 2-substituierten 2-oxazolinen mit einem anorganischen zinksalz |
-
0
- NL NL88380D patent/NL88380C/xx active
-
1952
- 1952-05-16 GB GB1241452A patent/GB730192A/en not_active Expired
-
1953
- 1953-05-13 ES ES0209289A patent/ES209289A1/es not_active Expired
- 1953-05-15 DE DE1953I0007251 patent/DE1000819C2/de not_active Expired
- 1953-05-15 FR FR1079351D patent/FR1079351A/fr not_active Expired
- 1953-05-16 BE BE520018A patent/BE520018A/fr unknown
- 1953-05-16 DK DK164353A patent/DK80450C/da active
- 1953-05-16 CH CH321108D patent/CH321108A/de unknown
- 1953-05-16 DK DK375153A patent/DK79734C/da active
Also Published As
| Publication number | Publication date |
|---|---|
| DE1000819B (de) | 1957-01-17 |
| CH321108A (de) | 1957-04-30 |
| DK80450C (da) | 1956-01-23 |
| DK79734C (da) | 1955-08-22 |
| FR1079351A (fr) | 1954-11-29 |
| DE1000819C2 (de) | 1957-06-27 |
| NL88380C (enrdf_load_stackoverflow) | |
| GB730192A (en) | 1955-05-18 |
| BE520018A (fr) | 1955-05-27 |
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