ES349860A1 - A method of preparation of chromogenic fatalids, fundamentally colorless or colored. (Machine-translation by Google Translate, not legally binding) - Google Patents

A method of preparation of chromogenic fatalids, fundamentally colorless or colored. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES349860A1
ES349860A1 ES349860A ES349860A ES349860A1 ES 349860 A1 ES349860 A1 ES 349860A1 ES 349860 A ES349860 A ES 349860A ES 349860 A ES349860 A ES 349860A ES 349860 A1 ES349860 A1 ES 349860A1
Authority
ES
Spain
Prior art keywords
substituted
radicals
see formula
chromogenic
fundamentally
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
ES349860A
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.)
NCR Voyix Corp
National Cash Register Co
Original Assignee
NCR Corp
National Cash Register Co
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 NCR Corp, National Cash Register Co filed Critical NCR Corp
Publication of ES349860A1 publication Critical patent/ES349860A1/en
Expired legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
    • B41M5/132—Chemical colour-forming components; Additives or binders therefor
    • B41M5/136—Organic colour formers, e.g. leuco dyes
    • B41M5/145—Organic colour formers, e.g. leuco dyes with a lactone or lactam ring
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B11/00—Diaryl- or thriarylmethane dyes
    • C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
    • C09B11/06—Hydroxy derivatives of triarylmethanes in which at least one OH group is bound to an aryl nucleus and their ethers or esters
    • C09B11/08—Phthaleins; Phenolphthaleins; Fluorescein
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B11/00—Diaryl- or thriarylmethane dyes
    • C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
    • C09B11/26—Triarylmethane dyes in which at least one of the aromatic nuclei is heterocyclic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Indole Compounds (AREA)
  • Color Printing (AREA)

Abstract

"A METHOD OF PREPARATION OF CHROMOGENIC, FUNDAMENTALLY COLORFUL OR LIGHTLY COLORED FATALIDES", characterized in that the structural formula is: ** (See formula) ** Where (see formula) and (see formula) represent mono or disubstituted indyl radicals, which have the structural formula ** (See formula) ** and carbazyl radicals, which have the structural formula: ** (See formula) ** Where R1, R2 and R3 represent alkyl radicals having no more than 5 carbon atoms, aryl and hydrogen radicals. Y and Z represent hydrogen and dialkylamino radicals having no more than 5 carbon atoms, taking into account that one of them (Y and Z) must be hydrogen, and the other the said dialkylamino radical. These phthalides are obtained by reacting a substituted R1-R2 indole or a R3 carbazole substituted with a dialkylaminophthalic anhydride in the presence of a metal halide and in an organic solvent, to obtain the corresponding substituted 3 (2-carboxy-dialkylaminobenzoyl) indole or carbazole. By reacting this intermediate product with a substituted R1 R2 indole, or with a substituted R3 carbazole, in the presence of a condensing agent, we will finally obtain the phthalide. (Machine-translation by Google Translate, not legally binding)
ES349860A 1967-01-30 1968-01-27 A method of preparation of chromogenic fatalids, fundamentally colorless or colored. (Machine-translation by Google Translate, not legally binding) Expired ES349860A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US61236967A 1967-01-30 1967-01-30

Publications (1)

Publication Number Publication Date
ES349860A1 true ES349860A1 (en) 1969-04-16

Family

ID=24452868

Family Applications (1)

Application Number Title Priority Date Filing Date
ES349860A Expired ES349860A1 (en) 1967-01-30 1968-01-27 A method of preparation of chromogenic fatalids, fundamentally colorless or colored. (Machine-translation by Google Translate, not legally binding)

Country Status (5)

Country Link
AT (1) AT271515B (en)
DK (1) DK121954B (en)
ES (1) ES349860A1 (en)
NO (1) NO126017B (en)
SE (1) SE325573B (en)

Also Published As

Publication number Publication date
AT271515B (en) 1969-06-10
NO126017B (en) 1972-12-11
DK121954B (en) 1971-12-27
SE325573B (en) 1970-07-06

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