GB884881A - Process for the manufacture of 2-amino-anthraquinone - Google Patents

Process for the manufacture of 2-amino-anthraquinone

Info

Publication number
GB884881A
GB884881A GB1449960A GB1449960A GB884881A GB 884881 A GB884881 A GB 884881A GB 1449960 A GB1449960 A GB 1449960A GB 1449960 A GB1449960 A GB 1449960A GB 884881 A GB884881 A GB 884881A
Authority
GB
United Kingdom
Prior art keywords
anthraquinone
amino
manufacture
tetrahydroanthraquinone
chloro
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
GB1449960A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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
Application filed by Ciba AG filed Critical Ciba AG
Publication of GB884881A publication Critical patent/GB884881A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
    • C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

2-Aminoanthraquinone is made by subjecting 2-chloro-1 : 4 : 11 : 12-tetrahydroanthraquinone at a temperature of at least 160 DEG C. and under superatmospheric pressure to the action of an aqueous solution of ammonia in the presence of an oxidising agent. Alcohol may also be present. 2-chloro-1 : 4 : 11 : 12-tetrahydroanthraquinone is made by reacting 1 : 4-naphthoquinone with 2-chlorobutadiene.
GB1449960A 1959-04-24 1960-04-25 Process for the manufacture of 2-amino-anthraquinone Expired GB884881A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH7252259A CH378344A (en) 1959-04-24 1959-04-24 Process for the preparation of 2-amino-anthraquinones

Publications (1)

Publication Number Publication Date
GB884881A true GB884881A (en) 1961-12-20

Family

ID=4531854

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1449960A Expired GB884881A (en) 1959-04-24 1960-04-25 Process for the manufacture of 2-amino-anthraquinone

Country Status (3)

Country Link
BE (1) BE590040A (en)
CH (1) CH378344A (en)
GB (1) GB884881A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6127580A (en) * 1995-09-06 2000-10-03 Basf Aktiengesellschaft Process for the preparation of substituted anthraquinones

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6127580A (en) * 1995-09-06 2000-10-03 Basf Aktiengesellschaft Process for the preparation of substituted anthraquinones

Also Published As

Publication number Publication date
BE590040A (en)
CH378344A (en) 1964-06-15

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