DD147105A5 - Verfahren zur einfuehrung von drei substituenten in das cyanurchlorid - Google Patents

Verfahren zur einfuehrung von drei substituenten in das cyanurchlorid Download PDF

Info

Publication number: DD147105A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; item; cyanuric chloride; atom; carbon atoms
Prior art date: 1978-11-20

Application number

DD79216465A

Other languages

German (de)

English (en)

Inventor

Klaus Hentschel

Friedrich Bittner

Original Assignee

Degussa

Priority date (The priority date 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 date listed.)

1978-11-20

Filing date

1979-10-25

Publication date

1981-03-18

1979-10-25 Application filed by Degussa filed Critical Degussa

1981-03-18 Publication of DD147105A5 publication Critical patent/DD147105A5/de

Links

MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 title claims abstract description 31
238000000034 method Methods 0.000 title claims abstract description 23
239000007788 liquid Substances 0.000 claims abstract description 34
238000006243 chemical reaction Methods 0.000 claims abstract description 10
239000002253 acid Substances 0.000 claims abstract description 9
239000011230 binding agent Substances 0.000 claims abstract description 5
239000007921 spray Substances 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 14
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 10
125000003342 alkenyl group Chemical group 0.000 claims description 8
150000001412 amines Chemical class 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
-1 pyrrolidino, morpholino Chemical group 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
239000003513 alkali Substances 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
150000001298 alcohols Chemical class 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
UAZDIGCOBKKMPU-UHFFFAOYSA-O azanium;azide Chemical class [NH4+].[N-]=[N+]=[N-] UAZDIGCOBKKMPU-UHFFFAOYSA-O 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
239000011261 inert gas Substances 0.000 claims description 2
229910052745 lead Inorganic materials 0.000 claims description 2
WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical group [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 claims description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 2
229910052753 mercury Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
229910052709 silver Inorganic materials 0.000 claims description 2
150000003378 silver Chemical group 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
229910052725 zinc Inorganic materials 0.000 claims description 2
239000011701 zinc Substances 0.000 claims description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000005219 aminonitrile group Chemical group 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
238000002844 melting Methods 0.000 claims 1
230000008018 melting Effects 0.000 claims 1
238000005507 spraying Methods 0.000 claims 1
239000000376 reactant Substances 0.000 abstract 2
230000001174 ascending effect Effects 0.000 abstract 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 4
239000000203 mixture Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000370 acceptor Substances 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
238000009826 distribution Methods 0.000 description 3
239000012530 fluid Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000002245 particle Substances 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 2
NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
KZKRRZFCAYOXQE-UHFFFAOYSA-N 1$l^{2}-azinane Chemical compound C1CC[N]CC1 KZKRRZFCAYOXQE-UHFFFAOYSA-N 0.000 description 1
UAGYXNZCZVTVJG-UHFFFAOYSA-N 3-amino-6-(2-phenylethenyl)benzene-1,2-disulfonic acid Chemical class OS(=O)(=O)C1=C(S(O)(=O)=O)C(N)=CC=C1C=CC1=CC=CC=C1 UAGYXNZCZVTVJG-UHFFFAOYSA-N 0.000 description 1
VSIXIFOXMNNBAM-UHFFFAOYSA-N 4-pyrrolidin-1-ylmorpholine Chemical compound C1CCCN1N1CCOCC1 VSIXIFOXMNNBAM-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
238000003723 Smelting Methods 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
238000005452 bending Methods 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
239000003595 mist Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
235000020095 red wine Nutrition 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
230000007704 transition Effects 0.000 description 1

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
- C07D251/26—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 only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J10/00—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor
- B01J10/02—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor of the thin-film type
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/26—Nozzle-type reactors, i.e. the distribution of the initial reactants within the reactor is effected by their introduction or injection through nozzles
- 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
- C07D251/26—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 only hetero atoms directly attached to ring carbon atoms
- C07D251/30—Only oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Physical Or Chemical Processes And Apparatus (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Treating Waste Gases (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD79216465A 1978-11-20 1979-10-25 Verfahren zur einfuehrung von drei substituenten in das cyanurchlorid DD147105A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2850338A DE2850338B2 (de)	1978-11-20	1978-11-20	Verfahren zur Herstellung von trisubstituierten s-Trianzinverbindungen

Publications (1)

Publication Number	Publication Date
DD147105A5 true DD147105A5 (de)	1981-03-18

Family

ID=6055172

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79216465A DD147105A5 (de)	1978-11-20	1979-10-25	Verfahren zur einfuehrung von drei substituenten in das cyanurchlorid

Country Status (19)

Country	Link
US (1)	US4281123A (fr)
JP (1)	JPS5573668A (fr)
AT (1)	AT368143B (fr)
BE (1)	BE880141A (fr)
BR (1)	BR7907283A (fr)
CA (1)	CA1131634A (fr)
CH (1)	CH644600A5 (fr)
DD (1)	DD147105A5 (fr)
DE (1)	DE2850338B2 (fr)
ES (1)	ES483875A1 (fr)
FR (1)	FR2441618A1 (fr)
GB (1)	GB2036735B (fr)
IL (1)	IL58607A (fr)
IN (1)	IN153838B (fr)
IT (1)	IT1119140B (fr)
NL (1)	NL7908437A (fr)
SE (1)	SE446730B (fr)
YU (1)	YU40229B (fr)
ZA (1)	ZA796281B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS58210072A (ja) *	1982-05-18	1983-12-07	チバ―ガイギ　アクチエンゲゼルシヤフト	塩化シアヌ−ルの水中懸濁物の製造または塩化シアヌ−ルとアンモニアまたはアミンとの反応のための方法および装置
US4552959A (en) *	1982-05-18	1985-11-12	Ciba Geigy Ag	Process for producing a suspension of cyanuric chloride in water
DE4016159A1 (de) *	1990-05-19	1991-11-21	Bayer Ag	Verfahren zur kontinuierlichen umsetzung von cyanurfluorid mit aminen sowie reaktor zur durchfuehrung des verfahrens
US5275745A (en) *	1993-02-22	1994-01-04	Exxon Research & Engineering Co.	Lubricant composition containing alkoxylated amine salt of trithiocyanuric acid
US5290460A (en) *	1993-02-22	1994-03-01	Exxon Research & Engineering Co.	Lubricant composition containing complexes of alkoxylated amine, trithiocyanuric acid, and adenine
US5420274A (en) *	1993-10-19	1995-05-30	Ciba-Geigy Corporation	Process for the preparation of 2,4-di(alkylamino)-6-alkylthio-s-triazines

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1670585U (de)	1953-11-13	1954-01-21	Erich Breyer	Einrichtung zum anfeuchten und feuchthalten von wickeln, umschlaegen od. dgl.
BE584306A (fr)	1958-11-05	1960-05-04	Geigy Ag J R	Nouveaux composés triaziniques à propriétés herbicides et leur préparation
NL131196C (fr)	1966-07-16
DD111378A5 (fr) *	1973-06-27	1975-02-12

1978
- 1978-11-20 DE DE2850338A patent/DE2850338B2/de not_active Withdrawn
1979
- 1979-07-16 YU YU1721/79A patent/YU40229B/xx unknown
- 1979-08-09 IT IT68647/79A patent/IT1119140B/it active
- 1979-08-29 IN IN900/CAL/79A patent/IN153838B/en unknown
- 1979-09-04 ES ES483875A patent/ES483875A1/es not_active Expired
- 1979-10-25 DD DD79216465A patent/DD147105A5/de unknown
- 1979-11-01 IL IL58607A patent/IL58607A/xx unknown
- 1979-11-09 BR BR7907283A patent/BR7907283A/pt unknown
- 1979-11-13 GB GB7939169A patent/GB2036735B/en not_active Expired
- 1979-11-16 US US06/094,873 patent/US4281123A/en not_active Expired - Lifetime
- 1979-11-19 CH CH1030479A patent/CH644600A5/de not_active IP Right Cessation
- 1979-11-19 AT AT0735279A patent/AT368143B/de not_active IP Right Cessation
- 1979-11-19 SE SE7909569A patent/SE446730B/sv not_active Application Discontinuation
- 1979-11-19 BE BE6/47015A patent/BE880141A/fr not_active IP Right Cessation
- 1979-11-19 NL NL7908437A patent/NL7908437A/nl not_active Application Discontinuation
- 1979-11-19 CA CA340,144A patent/CA1131634A/fr not_active Expired
- 1979-11-20 FR FR7928609A patent/FR2441618A1/fr active Granted
- 1979-11-20 JP JP14963179A patent/JPS5573668A/ja active Pending
- 1979-11-20 ZA ZA00796281A patent/ZA796281B/xx unknown

Also Published As

Publication number	Publication date
GB2036735A (en)	1980-07-02
CA1131634A (fr)	1982-09-14
ZA796281B (en)	1980-11-26
YU172179A (en)	1983-01-21
DE2850338B2 (de)	1981-05-07
JPS5573668A (en)	1980-06-03
IT1119140B (it)	1986-03-03
FR2441618A1 (fr)	1980-06-13
SE446730B (sv)	1986-10-06
ES483875A1 (es)	1980-05-16
YU40229B (en)	1985-08-31
IL58607A0 (en)	1980-02-29
DE2850338A1 (de)	1980-05-22
GB2036735B (en)	1983-03-09
US4281123A (en)	1981-07-28
AT368143B (de)	1982-09-10
ATA735279A (de)	1982-01-15
IL58607A (en)	1984-03-30
CH644600A5 (de)	1984-08-15
IT7968647A0 (it)	1979-08-09
FR2441618B1 (fr)	1983-08-05
BE880141A (fr)	1980-05-19
SE7909569L (sv)	1980-05-21
IN153838B (fr)	1984-08-18
NL7908437A (nl)	1980-05-22
BR7907283A (pt)	1980-09-23

Publication	Publication Date	Title
DE2850271C3 (de)	1981-10-01	Vorrichtung zur intensiven Mischung von Flüssigkeiten
DD147105A5 (de)	1981-03-18	Verfahren zur einfuehrung von drei substituenten in das cyanurchlorid
DE69812351T2 (de)	2004-02-19	Verfahren zur herstellung von melamin
DE2850331C2 (de)	1981-02-26	Verfahren zur Herstellung von ggf. substituierten 2-Amino-4,6-dichlors-triazinen
DD147054A5 (de)	1981-03-18	Verfahren zur herstellung von suspensionen oder loesungen von cyanurchlorid in wasser
DE2850332C2 (de)	1981-02-19	Verfahren zur Herstellung von substituierten 2-Mercapto-4,6-di-chlor-striazinen
EP0039478B1 (fr)	1984-10-24	Procédé et appareil de préparation d'oxyde de plomb technique
DE2850308C2 (de)	1984-09-20	Verfahren zur Herstellung von Suspensionen oder Lösungen von Cyanurchlorid in wasserhaltigen organischen Lösungsmitteln
DD147103A5 (de)	1981-03-18	Verfahren zur herstellung von 2-alkoxy-4,6-dichlor-s-triazinen
DE3919155A1 (de)	1990-01-11	Verfahren zum granulieren von fluessiger schlacke
DE2553931A1 (de)	1977-06-08	Verfahren und vorrichtung zur durchfuehrung von carbonylierungsreaktionen
DE2850243C2 (de)	1984-09-20	Verfahren zur Herstellung von Suspensionen von Cyanurchlorid in organischen Lösungsmitteln
DE2106200C3 (de)	1980-03-27	Verfahren zur Herstellung von 2-(4-Aminophenyl)-6-methyl-benzothiazol
EP0949252B1 (fr)	2001-04-25	Procédé pour la fabrication de pièces moulées de chlorure de cyanuryle
DE1533891C (de)	1971-11-11	Verfahren und Vorrichtung zum Sprühfrischen von kohlenstoffhaltigen Metallschmelzen, insbesondere Roheisenschmelzen
DE1931826A1 (de)	1971-01-14	Verfahren und Vorrichtung zur Herstellung von reinem Schwefeldioxid
AT204575B (de)	1959-07-25	Verfahren zum Konzentrieren von Harnstofflösungen
DE2138326A1 (de)	1972-03-09	Vorrichtung zur Durchführung einer Sulfonierungsreaktion
CH425741A (de)	1966-12-15	Kontinuierliches Verfahren zur Herstellung von Chlorcyan
DD271287A1 (de)	1989-08-30	Vorrichtung zur herstellung von pulver aus einer schmelze
DE1768216A1 (de)	1971-10-14	Verfahren zur Herstellung von Acrylsaeurenitril
EP0756589A1 (fr)	1997-02-05	Preparation sous forme pulverulente de semi-esters d'anhydrides cycliques d'acide dicarboxylique