GB853237A - Improvements relating to isoindolone dyes and their use - Google Patents

Improvements relating to isoindolone dyes and their use

Info

Publication number
GB853237A
GB853237A GB40492/58A GB4049258A GB853237A GB 853237 A GB853237 A GB 853237A GB 40492/58 A GB40492/58 A GB 40492/58A GB 4049258 A GB4049258 A GB 4049258A GB 853237 A GB853237 A GB 853237A
Authority
GB
United Kingdom
Prior art keywords
primary amino
araliphatic
cycloaliphatic
ammonia
aliphatic
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
GB40492/58A
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.)
Novartis AG
National Starch and Chemical Investment Holding Corp
Original Assignee
JR Geigy AG
National Starch and Chemical Investment Holding Corp
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 JR Geigy AG, National Starch and Chemical Investment Holding Corp filed Critical JR Geigy AG
Publication of GB853237A publication Critical patent/GB853237A/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
    • C09B57/00Other synthetic dyes of known constitution
    • C09B57/04Isoindoline dyes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/50Iso-indoles; Hydrogenated iso-indoles with oxygen and nitrogen atoms in positions 1 and 3

Abstract

The invention comprises isoindolines of the formula : <FORM:0853237/IV(b)/1> where Hal is a halogen atom, R is hydrogen, an aliphatic, cycloaliphatic, araliphatic or aromatic radical and n is 3 or 4. They are made by reacting a 2-cyano-benzoic acid ester containing 3 or 4 halogen substituents in the benzene ring with ammonia, an alkali-metal amide or a primary amine of the aliphatic, cycloaliphatic, araliphatic or aromatic series. Examples are given. The compounds are dyestuff intermediates. Specification 833,548 is referred to.ALSO:Coloured condensation products are made by reacting a 2-cyanobenzoic acid ester containing 3 or 4 halogen substituents in the benzene nucleus with ammonia, an alkali-metal amide or a primary amino and condensing the 3- iminoisoindoline -1- one obtained with a poly-primary amino compound of the homo- or hetero-cyclic aromatic series or hydrazino in the proportion of a molecular equivalent of the isoindoline for every primary amino group in the amine. The products are yellow, orange and red pigments and may be used for colouring plastics. Specification 833,548 is referred to.
GB40492/58A 1957-12-17 1958-12-16 Improvements relating to isoindolone dyes and their use Expired GB853237A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH853237X 1957-12-17

Publications (1)

Publication Number Publication Date
GB853237A true GB853237A (en) 1960-11-02

Family

ID=4542472

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40492/58A Expired GB853237A (en) 1957-12-17 1958-12-16 Improvements relating to isoindolone dyes and their use

Country Status (1)

Country Link
GB (1) GB853237A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2442229A1 (en) * 1978-11-24 1980-06-20 Asahi Chemical Ind 3-Imino-halogenated isoindolinone prepn. - by reacting halogenated phthalo-di:nitrile with water in the presence of hydrogen peroxide and ammonia and/or organic amine
GB2185482A (en) * 1986-01-15 1987-07-22 Ciba Geigy Ag Process for the preparation of alkyl esters of tetrachloro-2-cyanobenzoic acid
CN114196227A (en) * 2021-12-29 2022-03-18 百合花集团股份有限公司 Process for the preparation of isoindolinone pigments

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2442229A1 (en) * 1978-11-24 1980-06-20 Asahi Chemical Ind 3-Imino-halogenated isoindolinone prepn. - by reacting halogenated phthalo-di:nitrile with water in the presence of hydrogen peroxide and ammonia and/or organic amine
GB2185482A (en) * 1986-01-15 1987-07-22 Ciba Geigy Ag Process for the preparation of alkyl esters of tetrachloro-2-cyanobenzoic acid
GB2185482B (en) * 1986-01-15 1989-10-25 Ciba Geigy Ag Process for the preparation of alkyl esters of tetrachloro-2-cyanobenzoic acid
US4978768A (en) * 1986-01-15 1990-12-18 Ciba-Geigy Corporation Process for the preparation of alkyl esters of tetrachloro-2-cyano-benzoic acid
CN114196227A (en) * 2021-12-29 2022-03-18 百合花集团股份有限公司 Process for the preparation of isoindolinone pigments
CN114196227B (en) * 2021-12-29 2022-09-30 百合花集团股份有限公司 Process for the preparation of isoindolinone pigments

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