ATE213732T1 - METHOD FOR PRODUCING 2-(2,4-DIHYDROXYPHENYL)-4,6-BIS-(2,4-DIMETHYLPHENYL)-S TRIAZINE - Google Patents
METHOD FOR PRODUCING 2-(2,4-DIHYDROXYPHENYL)-4,6-BIS-(2,4-DIMETHYLPHENYL)-S TRIAZINEInfo
- Publication number
- ATE213732T1 ATE213732T1 AT96810845T AT96810845T ATE213732T1 AT E213732 T1 ATE213732 T1 AT E213732T1 AT 96810845 T AT96810845 T AT 96810845T AT 96810845 T AT96810845 T AT 96810845T AT E213732 T1 ATE213732 T1 AT E213732T1
- Authority
- AT
- Austria
- Prior art keywords
- compound
- formula
- mol
- formula iii
- cyanuric chloride
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/24—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
There is described a process for the preparation of 2-(2-4-dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-s-triazine of the formula I, which comprises (a) reacting cyanuric chloride of the formula II, in the presence of a Lewis acid in a ratio of 2.3 to 3.0 ml of Lewis acid per mole of cyanuric chloride employed in the presence of at least one inert chlorinated aromatic solvent, with 1,3-xylene of the formula III, in a ratio of 2.1 to 2.5 mol of compound of the formula III per mole of cyanuric chloride employed with addition of compound of the formula III in two steps, wherein the addition of 0.5 to 1.1 mol of the compound of the formula III takes place at 60 to 110 DEG C in the course of 2 to 12 hours, then the mixture is cooled to 20 to 50 DEG C in the course of 0 to 3 hours, after which the additional of 2.0 to 1.0 mol of the compound of the formula III takes place in the temperature range from 20 to 50 DEG C in the course of 5 to 15 hours to give the compound of the formula IV and then, (b) without isolating the compound of the formula IV obtained reacting this with resorcinol in a ratio of 0.5 to 1.0 mol of resorcinol per mole of cyanuric chloride employed at a temperature from 0 to 100 DEG C to give the compound of the formula I.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH354195 | 1995-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE213732T1 true ATE213732T1 (en) | 2002-03-15 |
Family
ID=4258215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT96810845T ATE213732T1 (en) | 1995-12-14 | 1996-12-03 | METHOD FOR PRODUCING 2-(2,4-DIHYDROXYPHENYL)-4,6-BIS-(2,4-DIMETHYLPHENYL)-S TRIAZINE |
Country Status (7)
Country | Link |
---|---|
KR (1) | KR100484265B1 (en) |
CN (1) | CN1070187C (en) |
AT (1) | ATE213732T1 (en) |
AU (1) | AU725423B2 (en) |
BR (1) | BR9605986A (en) |
DE (1) | DE59608792D1 (en) |
TW (1) | TW366340B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI259182B (en) * | 1998-11-17 | 2006-08-01 | Cytec Tech Corp | Process for preparing triazines using a combination of Lewis acids with reaction promoters |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1169947B (en) * | 1958-12-24 | 1964-05-14 | Ciba Geigy | Process for the preparation of 2- (2 ', 4'-dimethylphenyl) -4, 6-dichloro-1, 3, 5-triazine or 2, 4-di- (2', 4'-dimethylphenyl) -6-chloro- 1, 3, 5-triazine |
NL275368A (en) * | 1961-03-06 | |||
NL130993C (en) * | 1963-02-07 | |||
US4092466A (en) * | 1976-07-19 | 1978-05-30 | Nasa | Heat resistant polymers of oxidized styrylphosphine |
-
1996
- 1996-12-03 DE DE59608792T patent/DE59608792D1/en not_active Expired - Fee Related
- 1996-12-03 AT AT96810845T patent/ATE213732T1/en not_active IP Right Cessation
- 1996-12-04 TW TW085114935A patent/TW366340B/en active
- 1996-12-06 AU AU74217/96A patent/AU725423B2/en not_active Ceased
- 1996-12-12 CN CN96121532A patent/CN1070187C/en not_active Expired - Fee Related
- 1996-12-13 KR KR1019960067059A patent/KR100484265B1/en not_active IP Right Cessation
- 1996-12-13 BR BR9605986A patent/BR9605986A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR100484265B1 (en) | 2005-08-10 |
AU725423B2 (en) | 2000-10-12 |
MX9606261A (en) | 1997-10-31 |
DE59608792D1 (en) | 2002-04-04 |
AU7421796A (en) | 1997-06-19 |
BR9605986A (en) | 1998-09-01 |
TW366340B (en) | 1999-08-11 |
CN1161331A (en) | 1997-10-08 |
CN1070187C (en) | 2001-08-29 |
KR970042521A (en) | 1997-07-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
REN | Ceased due to non-payment of the annual fee |