GB1309621A - Disulphonylimides - Google Patents

Disulphonylimides

Info

Publication number
GB1309621A
GB1309621A GB1050471A GB1050471A GB1309621A GB 1309621 A GB1309621 A GB 1309621A GB 1050471 A GB1050471 A GB 1050471A GB 1050471 A GB1050471 A GB 1050471A GB 1309621 A GB1309621 A GB 1309621A
Authority
GB
United Kingdom
Prior art keywords
disulphonimides
formula
general formula
radical
organic
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
GB1050471A
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.)
Bayer AG
Original Assignee
Bayer 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
Priority claimed from DE19702021257 external-priority patent/DE2021257A1/en
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB1309621A publication Critical patent/GB1309621A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
    • C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
    • C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
    • C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
    • 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
    • C09B47/00—Porphines; Azaporphines
    • C09B47/04—Phthalocyanines abbreviation: Pc
    • C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
    • 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
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/523—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl amido or hydroxyalkyl amino sulfonyl group, a quaternised or non-quaternised amino alkyl sulfonyl amido group, or a substituted alkyl amino sulfonyl group, or a halogen alkyl sulfonyl amido or halogen alkyl amino sulfonyl group or a vinyl sulfonylamido or a substituted vinyl sulfonamido group

Abstract

1309621 Disulphonimides; betaines; sultams BAYER AG 21 April 1971 [30 April 1970] 10504/71 Heading C2C [Also in Division C4] The invention comprises disulphonimides of the general formula R 1 -(Z) n in which R 1 is a monovalent to tetravalent organic radical; Z is the radical -SO 2 NHSO 2 RX in which R represents an alkylene group containing at least 3 carbon atoms in a straight chain and X is a halogen; and n is an integer from 1 to 4 corresponding to the valency of R; and also their alkali metal, alkaline earth metal or ammonium salts. The disulphonimides may be prepared by reacting one mol of a sulphohalide of the general formula R 1 -(SO 2 -hal) n with n mols. of a sulphonamide of formula R 1 may be an optionally substituted alkyl, alkylene, aralkyl, aralkylene, cycloalkyl, cycloalkylene, oxy or arylene radical or monovalent to tetravalent radicals of a chromophor. Among the substituents mentioned are, halogen, sulphur, carboxyl, nitro, alkoxy, amino and acylamino. The disulphonimides may be reacted with amines for formula in which R 4 , R 5 and R 6 are hydrogen or alkyl to give betaines of the formula Sultams of the general formula may be prepared by heating one of the abovementioned disulphonylimide or a salt thereof in an aqueous, aqueous-organic or organic medium.
GB1050471A 1970-04-30 1971-04-21 Disulphonylimides Expired GB1309621A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19702021257 DE2021257A1 (en) 1970-04-30 1970-04-30 Disulfonylimides

Publications (1)

Publication Number Publication Date
GB1309621A true GB1309621A (en) 1973-03-14

Family

ID=5769922

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1050471A Expired GB1309621A (en) 1970-04-30 1971-04-21 Disulphonylimides

Country Status (4)

Country Link
BE (1) BE766548A (en)
FR (1) FR2091042A5 (en)
GB (1) GB1309621A (en)
NL (1) NL7105820A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4497741A (en) * 1981-12-09 1985-02-05 Ciba-Geigy Corporation Water-soluble zinc and aluminium phthalocyanines
US4566874A (en) * 1981-12-09 1986-01-28 Ciba-Geigy Corporation Water-soluble zinc and aluminium phthalocyanines and use thereof as photoactivators
WO1997023448A1 (en) * 1995-12-22 1997-07-03 Minnesota Mining And Manufacturing Company Preparation of bis(fluoroalkylenesulfonyl)imides and (fluoroalkylsulfonyl) (fluorosulfonyl)imides
JP2018043936A (en) * 2016-09-12 2018-03-22 東ソー・ファインケム株式会社 Bis-(4-haloethylbenzenesulfonyl)imide or its salt, method for producing the same and method for producing bis-(4-styrenesulfonyl)imide or its salt using bis-(4-haloethylbenzenesulfonyl)imide as precursor

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4497741A (en) * 1981-12-09 1985-02-05 Ciba-Geigy Corporation Water-soluble zinc and aluminium phthalocyanines
US4566874A (en) * 1981-12-09 1986-01-28 Ciba-Geigy Corporation Water-soluble zinc and aluminium phthalocyanines and use thereof as photoactivators
US5874616A (en) * 1995-03-06 1999-02-23 Minnesota Mining And Manufacturing Company Preparation of bis (fluoroalkylenesulfonyl) imides and (fluoroalkysulfony) (fluorosulfonyl) imides
WO1997023448A1 (en) * 1995-12-22 1997-07-03 Minnesota Mining And Manufacturing Company Preparation of bis(fluoroalkylenesulfonyl)imides and (fluoroalkylsulfonyl) (fluorosulfonyl)imides
JP2018043936A (en) * 2016-09-12 2018-03-22 東ソー・ファインケム株式会社 Bis-(4-haloethylbenzenesulfonyl)imide or its salt, method for producing the same and method for producing bis-(4-styrenesulfonyl)imide or its salt using bis-(4-haloethylbenzenesulfonyl)imide as precursor

Also Published As

Publication number Publication date
BE766548A (en) 1971-09-16
NL7105820A (en) 1971-11-02
FR2091042A5 (en) 1972-01-14

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees