GB549204A - Improvements in or relating to dyestuff intermediates - Google Patents

Improvements in or relating to dyestuff intermediates

Info

Publication number
GB549204A
GB549204A GB460441A GB460441A GB549204A GB 549204 A GB549204 A GB 549204A GB 460441 A GB460441 A GB 460441A GB 460441 A GB460441 A GB 460441A GB 549204 A GB549204 A GB 549204A
Authority
GB
United Kingdom
Prior art keywords
toluenesulphonate
quaternary ammonium
products
methyl
alkyl
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
GB460441A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB460441A priority Critical patent/GB549204A/en
Publication of GB549204A publication Critical patent/GB549204A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62—Benzothiazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62—Benzothiazoles
    • C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

549,204. Thioesters. KENDALL, J. D. April 7, 1941, No. 4604. Samples furnished. [Class 2 (iii)] Dyestuff intermediates are prepared by condensing a quaternary ammonium salt of a heterocyclic nitrogen compound containing a reactive methyl or mono alkyl substituted methyl group in α or y position with an excess of a compound having the formula S = C(SR) 2 wherein R is an alkyl or aralkyl group in the presence of a base and a solvent. In examples, dimethyltrithiocarbonate is condensed in the presence of triethylamine and alcohol with 1 - methylbenzthiazolmethyltoluenesulphonate, quinaldinemethiodide, 4:5-dimethoxy-1-methyl benzthiazolethyl - p - toluenesulphonate and 1:4 - dimethylbenzthiazolethyl - p toluenesulphonate. By treating the products with alkyl or aralkyl esters, quaternary ammonium salts which are also intermediates are obtained (cf. Specification 549,202). Dyestuffs in small quantities are obtained together with the products (cf. Specification 549,203). Quaternary ammonium salts containing reactive methyl groups for use as starting materials may be derived from oxazoles, selenazoles and thiazoles of the benzene, naphthalene, acenaphthene and anthracene series, pyridine and its polycyclic homologues indolenines, pyrimidines, quinazolines, thio- #:#<SP>1</SP>-diazol, oxazolines, thiazolines, selenazolines and their amino, hydroxy, alkoxy, methylenedioxy and halogen substitution derivatives. Samples have been furnished under Sect. 2 (5) of products obtained by condensing (1) dimethyltrithiocarbonate with 1-ethylbenzthiazolmethyl - p - toluenesulphonate and (2) dibenzyltrithiocarbonate with 1-methylbenzthiazolmethyl-p-toluenesulphonate. Dibenzyltrithiocarbonate is obtained by treating with benzylchloride the aqueous potassium trithiocarbonate prepared by dissolving in water the product obtained by reacting carbondisulphide with alcoholic potash saturated with hydrogen sulphide.
GB460441A 1941-04-07 1941-04-07 Improvements in or relating to dyestuff intermediates Expired GB549204A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB460441A GB549204A (en) 1941-04-07 1941-04-07 Improvements in or relating to dyestuff intermediates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB460441A GB549204A (en) 1941-04-07 1941-04-07 Improvements in or relating to dyestuff intermediates

Publications (1)

Publication Number Publication Date
GB549204A true GB549204A (en) 1942-11-11

Family

ID=9780304

Family Applications (1)

Application Number Title Priority Date Filing Date
GB460441A Expired GB549204A (en) 1941-04-07 1941-04-07 Improvements in or relating to dyestuff intermediates

Country Status (1)

Country Link
GB (1) GB549204A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450400A (en) * 1944-01-26 1948-09-28 Gen Aniline & Film Corp Process for producing dye intermediates
US2471996A (en) * 1945-01-19 1949-05-31 Gen Aniline & Film Corp Trinuclear iminol cyanine dyes
US4376817A (en) * 1978-09-01 1983-03-15 Ciba-Geigy Ag Direct-positive photographic material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450400A (en) * 1944-01-26 1948-09-28 Gen Aniline & Film Corp Process for producing dye intermediates
US2471996A (en) * 1945-01-19 1949-05-31 Gen Aniline & Film Corp Trinuclear iminol cyanine dyes
US4376817A (en) * 1978-09-01 1983-03-15 Ciba-Geigy Ag Direct-positive photographic material

Similar Documents

Publication Publication Date Title
US3741989A (en) Lactonic acetals
GB1332477A (en) Basic azo dyes free from sulphonic acid groups their production and use
GB1448852A (en) Plant growth inhibiting diamino-5-nitropyrimidines
GB549204A (en) Improvements in or relating to dyestuff intermediates
GB549202A (en) Improvements in or relating to dyestuffs and dyestuff intermediates
GB1212174A (en) Process for the production of new 2-oxo-1,2-dihydroquinoline derivatives
US2334711A (en) Ctanine dyestdff intermediates
US2332517A (en) Ctanine djtesttjff intermediates
GB654690A (en) Improvements in cyanine dyes and photographic emulsions containing the same
GB549203A (en) Improvements in or relating to dyestuffs
GB1423073A (en) Amines and processes for their manufacture
GB1411474A (en) Coumarin and coumarinimide derivatives
GB549201A (en) Improvements in or relating to dyestuff intermediates
GB1514895A (en) Substituted aminobenzaldehyde compounds containing a sulphonamide residue and processes for their manufacture
GB610569A (en) Improvements in or relating to the production of dyes and the sensitisation of photographic emulsions
GB553143A (en) Improvements in or relating to the production of organic compounds especially intended for use as dyestuff intermediates
GB1102891A (en) Process for the preparation of heterocyclammonium betaines
US2518475A (en) Dyestuffs
GB778221A (en) Improvements in or relating to photographic sensitizers
GR13983B (en) METHOD OF PREPARATION OF SUBSTITUTED OXAZOL - 5 - ONIS COMPOUNDS.
GB426718A (en) Improvements in or relating to the production of dyestuffs
YU48445B (en) PROCEDURE FOR OBTAINING NEW 4-HYDROXYCUMARINE AND 1 3-INDANDION DERIVATIVES
GB587810A (en) Improvements relating to the production of substituted carboxylic amides
GB553144A (en) Improvements in and relating to dyestuffs, especially for use as photographic sensitising dyestuffs
GB727481A (en) Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x