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Patent · US4435324A · A · US

Process for the preparation of 1-alkylaminoanthraquinones

(11) Publication number
US4435324A
(21) Application number
US-36169282-A
(22) Filing date
1982-03-25
(30) Priority date
1981-04-16
(43) Publication date
1984-03-06
(45) Date of grant
1984-03-06
(52) CPC
  • C09B Organic dyes or closely-related compounds for producing dyes {, e.g. pigments}; mordants; lakes: 1/285
(73) Assignee
BAYER AG
(54) Title
Process for the preparation of 1-alkylaminoanthraquinones
(57) Abstract

Improved process for the preparation of 1-alkylaminoanthraquinones by aminolysis of 1-nitroanthraquinones with alkylamines at elevated temperature in water and organic water-immiscible solvents, in the presence of acid-binding agents, according to which process calcium hydroxide is used as the acid-binding agent.

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Claims (8)

  1. In the process for the preparation of 1-alkylaminoanthraquinones, wherein 1-nitroanthraquinones are aminolysed with alkylamines at elevated temperature in water and organic water-immiscible solvents, in the presence of acid-binding agents, the improvement comprising using calcium hydroxide as the acid-binding agent.
  2. The process of claim 1, wherein the calcium hydroxide is employed in quantities of from 1 to 5 equivalents per mol of 1-nitroanthraquinone.
  3. The process of claim 1, wherein the alkylamines are used in quantities of from 1 to 1.5 mol per mol of 1-nitroanthraquinone.
  4. The process of claim 1, wherein the alkylamines are used in quantities of from 1.05 to 1.2 mol per mol of 1-nitroanthraquinone.
  5. The process of claim 1, wherein the reaction mixture produced after the end of the aminolysis is heated to the reflux temperature with ammonium salts until nitrite is no longer detectable in the reaction mixture.
  6. The process of claim 5, wherein as the ammonium salts are used salts of those acids which form water-soluble salts with calcium.
  7. The process of claim 5, wherein the ammonium salts are employed in quantities which are at least equivalent to the quantity of calcium hydroxide used.
  8. The process of claim 5, wherein from 2 to 6 equivalents of ammonium salts are employed per mol of calcium hydroxide used.

Citations (5)

  • US1404056A
  • US1931295A
  • US2185709A
  • US4046785A
  • US4163947A
Record as JSON
{
  "publication_number": "US4435324A",
  "country": "US",
  "kind": "A",
  "title": "Process for the preparation of 1-alkylaminoanthraquinones",
  "abstract": "Improved process for the preparation of 1-alkylaminoanthraquinones by aminolysis of 1-nitroanthraquinones with alkylamines at elevated temperature in water and organic water-immiscible solvents, in the presence of acid-binding agents, according to which process calcium hydroxide is used as the acid-binding agent.",
  "claims": [
    "1. In the process for the preparation of 1-alkylaminoanthraquinones, wherein 1-nitroanthraquinones are aminolysed with alkylamines at elevated temperature in water and organic water-immiscible solvents, in the presence of acid-binding agents, the improvement comprising using calcium hydroxide as the acid-binding agent.",
    "2. The process of claim 1, wherein the calcium hydroxide is employed in quantities of from 1 to 5 equivalents per mol of 1-nitroanthraquinone.",
    "3. The process of claim 1, wherein the alkylamines are used in quantities of from 1 to 1.5 mol per mol of 1-nitroanthraquinone.",
    "4. The process of claim 1, wherein the alkylamines are used in quantities of from 1.05 to 1.2 mol per mol of 1-nitroanthraquinone.",
    "5. The process of claim 1, wherein the reaction mixture produced after the end of the aminolysis is heated to the reflux temperature with ammonium salts until nitrite is no longer detectable in the reaction mixture.",
    "6. The process of claim 5, wherein as the ammonium salts are used salts of those acids which form water-soluble salts with calcium.",
    "7. The process of claim 5, wherein the ammonium salts are employed in quantities which are at least equivalent to the quantity of calcium hydroxide used.",
    "8. The process of claim 5, wherein from 2 to 6 equivalents of ammonium salts are employed per mol of calcium hydroxide used."
  ],
  "cpc": [
    "C09B 1/285"
  ],
  "assignees": [
    "BAYER AG"
  ],
  "filing_date": "1982-03-25",
  "publication_date": "1984-03-06",
  "grant_date": "1984-03-06",
  "priority_date": "1981-04-16",
  "application_number": "US-36169282-A",
  "family_id": "6130351",
  "citations": [
    "US1404056A",
    "US1931295A",
    "US2185709A",
    "US4046785A",
    "US4163947A"
  ]
}

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