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GB914719A - New derivatives of coumarin - Google Patents

New derivatives of coumarin

Info

Publication number
GB914719A
GB914719A GB283461A GB283461A GB914719A GB 914719 A GB914719 A GB 914719A GB 283461 A GB283461 A GB 283461A GB 283461 A GB283461 A GB 283461A GB 914719 A GB914719 A GB 914719A
Authority
GB
United Kingdom
Prior art keywords
compounds
coumarin
carbon atoms
alkyl group
acid
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
GB283461A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB914719A publication Critical patent/GB914719A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C09B57/00Other synthetic dyes of known constitution
    • C09B57/02Coumarine dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Coloring (AREA)

Abstract

In Example 7 a mixture of polyvinyl chloride, dioctyl phthalate, titanium dioxide and 3-(5-methyl-benzoxazolyl-(2))-coumarin is made into a foil by rolling at 150 DEG -155 DEG C. on a two-roll calender. Other suitable coumarin derivatives are those of the formula <FORM:0914719/IV(a)/1> wherein R1, R3 and R4 each represent a hydrogen or chlorine atom or an alkyl group containing 1-4 carbon atoms, and R2 represents a hydrogen atom or an alkyl group containing 1-4 carbon atoms (see Group IV(b)). The compounds are optical brightening agents.ALSO:The invention comprises coumarin derivatives of the formula <PICT:0914719/IV (b)/1> wherein R1, R3 and R4 may be identical or different and represent a hydrogen or a chlorine atom or an alkyl group containing 1-4 carbon atoms, and R2 represents an alkyl group containing 1-4 carbon atoms. The compounds are prepared by the action of a watereliminating agent on (1) a coumarin-3-carboxylic acid and an ortho-amino-phenol of formulae <PICT:0914719/IV (b)/2> or (2) an intermediate amide or ester obtainable from reaction between the acid above or its functional derivatives and the aminophenol. Preferred compounds are those in which R1, R3 and R4 each represent a hydrogen or chlorine atom or a methyl group, these substituents being in the 6-position of the coumarin residue and in the 5- and 6-positions of the benzoxazole residue, and R2 represents a hydrogen atom or a methyl group. Suitable water-eliminating agents are zinc chloride, phosphoric acids of the formula Hn+2PnO3n+1 where n is an integer preferably greater than 1, mixtures of these phosphoric acids, or concentrated aqueous or anhydrous sulphuric acid. An elevated temperature is preferable for the water-eliminating step. Examples (1)-(4) describe the preparation of numerous compounds of the preferred class. In Example (5) an intermediate acylamino compound is prepared and is then cyclized. The intermediate coumarin-3-carboxylic acids are prepared by condensing the corresponding ortho-hydroxy-benzaldehyde or -phenyl ketone with (1) malonic acid, or (2) with malononitrile to give the corresponding nitrile which is then hydrolysed to the acid. The products may be used as light-filters for ultra-violet rays, as intermediates in the manufacture of dyestuffs, for photographic purposes, and as optical brightening agents for fibres and fabrics (see Groups IV(a) and IV(c)).ALSO:Compounds of the general formula <FORM:0914719/IV (b)/1> wherein R1, R3 and R4 each represent a hyd rogen or chlorine atom or an alkyl group containing 1-4 carbon atoms, and R2 represents a hydrogen atom or an alkyl group containing 1-4 carbon atoms (see Group IV(b)), may be used as optical brightening agents for fibres and fabrics, especially polyester fibres and polyester, polyamide and acetate rayon fabrics. The compounds may be applied to polyester fibres by known methods, e.g. in a fine dispersion from an aqueous bath. In Example (6) a polyester fabric is treated in a bath containing aqueous formic acid and one of the above compounds. In Example (8) a polyamide acetic acid and one of the above compounds; fabric is treated in a bath containing aqueous acetate rayon fabric may be treated similarly.
GB283461A 1960-02-05 1961-01-24 New derivatives of coumarin Expired GB914719A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH127760A CH390918A (en) 1960-02-05 1960-02-05 Process for the production of new coumarin derivatives

Publications (1)

Publication Number Publication Date
GB914719A true GB914719A (en) 1963-01-02

Family

ID=4206645

Family Applications (1)

Application Number Title Priority Date Filing Date
GB283461A Expired GB914719A (en) 1960-02-05 1961-01-24 New derivatives of coumarin

Country Status (6)

Country Link
BE (1) BE599311A (en)
CH (1) CH390918A (en)
DE (1) DE1222014B (en)
ES (1) ES264659A1 (en)
GB (1) GB914719A (en)
NL (1) NL260844A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015063490A (en) * 2013-09-25 2015-04-09 クラレノリタケデンタル株式会社 Compound suitable for organic fluorescent dye and curable composition containing the same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1238873B (en) * 1961-07-19 1967-04-20 Ciba Geigy Optical brighteners

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB522672A (en) * 1939-06-02 1940-06-24 Meyer Hans Treating articles, substances or materials of a yellowish or off-white tint so as to obtain a pure white appearance
FR1159273A (en) * 1955-09-28 1958-06-25 Bayer Ag Brightening agents

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015063490A (en) * 2013-09-25 2015-04-09 クラレノリタケデンタル株式会社 Compound suitable for organic fluorescent dye and curable composition containing the same

Also Published As

Publication number Publication date
CH390918A (en) 1965-04-30
DE1222014B (en) 1966-08-04
BE599311A (en)
ES264659A1 (en) 1961-08-01
NL260844A (en)

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