ES386268A1 - Stilbene compounds - Google Patents

Stilbene compounds

Info

Publication number
ES386268A1
ES386268A1 ES386268A ES386268A ES386268A1 ES 386268 A1 ES386268 A1 ES 386268A1 ES 386268 A ES386268 A ES 386268A ES 386268 A ES386268 A ES 386268A ES 386268 A1 ES386268 A1 ES 386268A1
Authority
ES
Spain
Prior art keywords
formula
chosen
moles
mol
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
Application number
ES386268A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sandoz AG
Original Assignee
Sandoz AG
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.)
Filing date
Publication date
Application filed by Sandoz AG filed Critical Sandoz AG
Publication of ES386268A1 publication Critical patent/ES386268A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B23/00Methine or polymethine dyes, e.g. cyanine dyes
    • C09B23/14Styryl dyes
    • C09B23/148Stilbene dyes containing the moiety -C6H5-CH=CH-C6H5
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Coloring (AREA)
  • Detergent Compositions (AREA)

Abstract

Procedure for obtaining stilbene derivatives, of general formula **(See formula)** where X and Y, independent of each other, mean in each case a phenylemino residue, which can be substituted, and both a residue of the formula **(See formula)** how much formula **(See formula)** T and Z each signify both a residue of formula (II) and (III), R is chosen from hydrogen and low molecular weight alkyl, which may be substituted by hydroxy, alkoxy, cyano, aminocarbonyl, phenyl, phenoxy and cresoxy, R1 is chosen from hydrogen and a low molecular weight alkyl moiety, R2 means hydroxy, cyano, -CO-CmH2m + 1, (see formula) as well as -COOR7, R3 and R4, independent of each other, mean in each case both a low molecular weight alkyl moiety, and hydroxyalkyl as R3 and R4, together with the nitrogen atom, form a saturated heterocyclic moiety, R5 and R6, independent of each other, are chosen from a hydrogen atom, a low molecular weight alkyl moiety and a hydroxyalkyl group, since R5 and R6, together with the nitro-hay atom, form a saturated heterocyclic moiety, R7 stands for a low molecular weight alkyl moiety which may be substituted by hydroxy, alkoxy, phenoxy, cresoxy as well as phenyl, Me represents an equivalent of a metal chosen from an alkali and alkaline earth metal as well as an ammonium group. Anion is a colorless anion and m is a number from 1 to 3, n is chosen from 1 to 2 and p is a number from 2 to 6, with all residues being able **(See formula)** in the substituents T, X, Y and Z, they are the same as well as different from each other and all the residues R3 to R6, likewise, the same and also different from each other, the molecule presenting only two sulfonic radicals linked to the stilbene moiety, characterized in that in arbitrary sequence, both 2 moles of a cyanuric halide are reacted with a) 1 mole of 4,4'-diaminoestilben-2,2'-disulfonic acid, which may be in the form of a salt, b) 0 to 2 moles of an aminobenzene, which may be substituted and c) 2 to 4 moles of an amine of formula **(See formula)** both in the single state and in the form of a mixture of amines of formula (IV); the amines mentioned under b) and c) totaling 4 moles, the reaction product being reacted with a compound chosen from an acid and a quaternizing agent; as 1 mol of a cyanuric halide is reacted with a) 1 mol of acid chosen from 4-amino-4'-nitro- acid and 4-amino-4'-acylaminoestilben-2,2'-disulfonic acid, which may be in the form of a salt, b) 0 to 1 mol of an aminobenzene, which may be substituted, c) 1 to 2 mol of an amine of formula (IV) both in the single state and in the form of a mixture of amines of formula (IV), bringing the amines mentioned under b) and c) to a total of 2 moles, then the nitro group is reduced, just as the acylamino group is hydrolyzed and the amino group is reacted with 1 mole of a cyanuric halide and the compound Dihalogenotriazinioic acid is reacted in arbitrary sequence with d) 0 to 1 mol of an aminobenzene, which may be substituted, and e) 1 to 2 mol of an amine of formula (IV), both in the single state and in the form of a mixture of amines of formula (IV), the amines mentioned under d) and e) amounting to a total of 2 moles, being able to react the product reaction with a compound chosen from an acid and a quaternizing agent. (Machine-translation by Google Translate, not legally binding)
ES386268A 1969-12-11 1970-12-09 Stilbene compounds Expired ES386268A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1842569A CH529770A (en) 1969-12-11 1969-12-11 Process for the preparation of new stilbene compounds

Publications (1)

Publication Number Publication Date
ES386268A1 true ES386268A1 (en) 1974-01-01

Family

ID=4432886

Family Applications (1)

Application Number Title Priority Date Filing Date
ES386268A Expired ES386268A1 (en) 1969-12-11 1970-12-09 Stilbene compounds

Country Status (10)

Country Link
US (1) US3757010A (en)
JP (2) JPS527011B1 (en)
BE (1) BE760178A (en)
CH (1) CH529770A (en)
DE (1) DE2060085A1 (en)
ES (1) ES386268A1 (en)
FR (1) FR2073529A5 (en)
GB (1) GB1299120A (en)
NL (1) NL7018032A (en)
ZA (1) ZA708379B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH597204A5 (en) * 1973-02-16 1978-03-31 Sandoz Ag
CH583211A5 (en) * 1973-05-22 1976-12-31 Sandoz Ag
CH583212A5 (en) * 1973-07-02 1976-12-31 Sandoz Ag
CH603878B5 (en) * 1973-09-21 1978-08-31 Hoechst Ag
CH590965A5 (en) * 1973-12-19 1977-08-31 Ciba Geigy Ag
DE2712686C2 (en) * 1977-03-23 1986-09-04 Bayer Ag, 5090 Leverkusen 4-Triazinyl-4'-benzoxazolyl or 4'-phenyl-stilbene derivatives
US4478598A (en) * 1981-02-26 1984-10-23 Ciba-Geigy Corporation Amphoteric styrene derivatives useful as fluorescent brighteners
DE3922494A1 (en) * 1989-07-08 1991-01-17 Bayer Ag FLUESSIGWASCHMITTEL
US5319126A (en) * 1993-01-29 1994-06-07 Akzo N.V. α-aminonitriles derived from fatty alkyl alkylene diamines
GB9930247D0 (en) * 1999-12-22 2000-02-09 Clariant Int Ltd Improvements in or relating to organic compounds
GB9930177D0 (en) * 1999-12-22 2000-02-09 Clariant Int Ltd Improvements in or relating to organic compounds
JP2005529854A (en) * 2002-03-19 2005-10-06 チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド Amphoteric and cationic fluorescent whitening agents
EP1511901B1 (en) * 2002-06-11 2007-07-04 Ciba SC Holding AG Whitening pigments
CN102898855B (en) * 2012-09-29 2013-12-11 山东大学 Synthesis and application of cetyl or octadecyl dimethyl tertiary amine quaternary ammonium salt high performance fluorescent whitening agent having amino acid structure

Also Published As

Publication number Publication date
CH529770A (en) 1972-10-31
JPS4924127B1 (en) 1974-06-20
JPS527011B1 (en) 1977-02-26
BE760178A (en) 1971-05-17
FR2073529A5 (en) 1971-10-01
GB1299120A (en) 1972-12-06
ZA708379B (en) 1972-07-26
NL7018032A (en) 1971-06-15
DE2060085A1 (en) 1971-06-16
US3757010A (en) 1973-09-04

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