GB378942A - Improvements in and relating to the production of dibenzanthrone derivatives - Google Patents

Improvements in and relating to the production of dibenzanthrone derivatives

Info

Publication number
GB378942A
GB378942A GB1481631A GB1481631A GB378942A GB 378942 A GB378942 A GB 378942A GB 1481631 A GB1481631 A GB 1481631A GB 1481631 A GB1481631 A GB 1481631A GB 378942 A GB378942 A GB 378942A
Authority
GB
United Kingdom
Prior art keywords
dihydroxydibenzanthrone
prepared according
dyes
paraformaldehyde
class
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
GB1481631A
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.)
IAN BLOHM ANDERSON
PETER GEORGE CARTER
ROBERT FRASER THOMSON
Imperial Chemical Industries Ltd
Original Assignee
IAN BLOHM ANDERSON
PETER GEORGE CARTER
ROBERT FRASER THOMSON
Imperial Chemical Industries Ltd
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 IAN BLOHM ANDERSON, PETER GEORGE CARTER, ROBERT FRASER THOMSON, Imperial Chemical Industries Ltd filed Critical IAN BLOHM ANDERSON
Priority to GB1481631A priority Critical patent/GB378942A/en
Publication of GB378942A publication Critical patent/GB378942A/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
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/22Dibenzanthrones; Isodibenzanthrones
    • C09B3/30Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Dibenzanthrone derivatives.--Blue and reddish-blue dyestuffs are obtained by treating a diacyl derivative of Bz2.Bz2<1>-dihydroxydibenzanthrone obtained by acylating according to Specification 193,431, [Class 2 (iii), Dyes &c.], or a dialkyl derivative of Bz2.Bz2<1>-dihydroxydibenzanthrone obtained by alkylating according to examples A and B (jointly) of Specification 181,304, (the Bz2: Bz2<1>-dihydroxydibenzanthnone obtained according to example 13 of Specification 203,533, [Class 2 (iii), Dyes &c.], being the parent material in each case), with an aliphatic aldehyde, or a p substance yielding such an aldehyde, in a sulphuric acid medium. Formaldehyde or paraformaldehyde is preferably employed in concentrated sulphuric acid, and in the case of the diacyl derivatives the acyl groups appear to be split off with formation of the methylene ethers. Similar alkylidene ethers appear to be formed when higher aldehydes are employed, and also when the dialkyl deriva ives are treated. In the latter case the dimethyl derivative is preferably employed, for example in the pure form of Caledon Jade Green. In examples: (1) Bz2 : Bz2<1>-diacetoxydibenzanthrone (prepared according to example 3 of Specification 193,431 from the Bz2 : Bz2<1>-dihydroxydibenzanthrone prepared according to example 13 of Specification 203,533) is treated with paraformaldehyde in sulphuric acid; cotton is dyed bright blue shades by the product: (2) Bz2 : Bz2<1>-dihydroxydibenzanthrone dibenzoate (prepared according to example 2 of Specification 193,431 from the Bz2 : Bz2<1>-dihydroxydibenzanthrone prepared according to example 13 of Specification 203,533) is treated as in (1) to give a similar product: (3) Bz2 : Bz2<1>-dimethoxydibenzanthrone (prepared according to example B of Specification 181,304, [Class 2 (iii), Dyes &c.], from the dihydroxydibenzanthrone obtained according to example 13 of Specification 203,533) is treated with paraformaldehyde in concentrated sulphuric acid to give a product dyeing reddish-blue shades; by replacing paraformaldehyde by paracetaldehyde a similar dyestuff is obtained. Specification 206,638, [Class 2 (iii), Dyes &c.], also is referred to.
GB1481631A 1931-05-19 1931-05-19 Improvements in and relating to the production of dibenzanthrone derivatives Expired GB378942A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1481631A GB378942A (en) 1931-05-19 1931-05-19 Improvements in and relating to the production of dibenzanthrone derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1481631A GB378942A (en) 1931-05-19 1931-05-19 Improvements in and relating to the production of dibenzanthrone derivatives

Publications (1)

Publication Number Publication Date
GB378942A true GB378942A (en) 1932-08-19

Family

ID=10047981

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1481631A Expired GB378942A (en) 1931-05-19 1931-05-19 Improvements in and relating to the production of dibenzanthrone derivatives

Country Status (1)

Country Link
GB (1) GB378942A (en)

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