GB345250A - Improvements in and relating to the recovery and purification of alkaloids from cocoa products - Google Patents

Improvements in and relating to the recovery and purification of alkaloids from cocoa products

Info

Publication number
GB345250A
GB345250A GB3032229A GB3032229A GB345250A GB 345250 A GB345250 A GB 345250A GB 3032229 A GB3032229 A GB 3032229A GB 3032229 A GB3032229 A GB 3032229A GB 345250 A GB345250 A GB 345250A
Authority
GB
United Kingdom
Prior art keywords
theobromine
added
lime
acid
separated
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
GB3032229A
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.)
Monsanto Chemical Works Ltd
Original Assignee
Monsanto Chemical Works 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 Monsanto Chemical Works Ltd filed Critical Monsanto Chemical Works Ltd
Priority to GB3032229A priority Critical patent/GB345250A/en
Publication of GB345250A publication Critical patent/GB345250A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/12Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1, 3, and 7, e.g. caffeine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/10Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 3 and 7, e.g. theobromine

Landscapes

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

Abstract

Theobromine and caffeine.-Cocoa products are subjected, in aqueous suspension, to the action of a mineral acid such as sulphuric, hydrochloric or phosphoric acid or an acid anhydride such as sulphur dioxide preferably at the boiling point. An alkaline substance such as lime or other alkaline earth oxide or hydroxide is then added in quantity at least sufficient to neutralize the acidity and after the solid cocoa material has been separated, the alkaloids are recovered from the resulting liquors. The acid treatment may also be carried out at higher temperatures under pressure. If just sufficient lime &c. has been added to neutralize the acidity, additional alkali in the form of a weak base such as ammonium hydroxide may be added. When excess of alkali has been used, the solids may be separated by filtration and theobromine may be precipitated from the filtrate by the addition of substances such as hydrochloric acid; carbon dioxide may also be used, the liquid being filtered hot from the precipitated calcium carbonate, theobromine crystallizing on cooling. As this precipitation of calcium carbonate has a purifying action, sodium carbonate or the like can be added to the extract before or after the addition of carbon dioxide to produce further calcium carbonate by reaction with the soluble calcium salts present. The mother liquor remaining after the separation of the theobromine may be evaporated and a second crop of theobromine crystals thus obtained. The second mother liquor may be treated for the recovery of caffeine, for example by extraction with organic solvents such as benzol. The impure second crop of theobromine crystals may be purified by treating an aqueous solution thereof with calcium or alkali hydroxide, and precipitating theobromine by acidification after filtering the solution; or the solution may be treated with an alkali carbonate such as sodium carbonate and filtered from the resulting alkaline earth carbonate before acidification. The extracted liquors may be mixed with the separated solid cocoa material, the wet material being directly used as a fertilizer, or it can be dried and ground and used as a fertilizer or cattle food. The drying is preferably done by means of the gases as their carbon dioxide content neutralizes the free lime in the material.ALSO:Cocoa products are subjected, in aqueous suspension, to the action of a mineral acid such as sulphuric, hydrochloric or phosphoric acid, or an acid anhydride such as sulphur dioxide preferably at the boiling-point. An alkaline substance such as lime or other alkaline-earth oxide or hydroxide is then added in quantity at least sufficient to neutralize the acidity and after the solid cocoa material has been separated, the alkaloids are recovered from the resulting liquors. The extracted liquors may be mixed with the separated solid cocoa material, the wet material being directly used as a fertilizer, or it can be dried and ground and used as a fertilizer or cattle food. The drying is preferably done by means of flue gases as their carbon dioxide content neutralizes the free lime in the material.
GB3032229A 1929-10-07 1929-10-07 Improvements in and relating to the recovery and purification of alkaloids from cocoa products Expired GB345250A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3032229A GB345250A (en) 1929-10-07 1929-10-07 Improvements in and relating to the recovery and purification of alkaloids from cocoa products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3032229A GB345250A (en) 1929-10-07 1929-10-07 Improvements in and relating to the recovery and purification of alkaloids from cocoa products

Publications (1)

Publication Number Publication Date
GB345250A true GB345250A (en) 1931-03-09

Family

ID=10305796

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3032229A Expired GB345250A (en) 1929-10-07 1929-10-07 Improvements in and relating to the recovery and purification of alkaloids from cocoa products

Country Status (1)

Country Link
GB (1) GB345250A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7368144B2 (en) 2000-08-11 2008-05-06 Barry Callebaut France Method for obtaining cocoa bean polyphenol extracts, resulting extracts and uses thereof
US7820713B2 (en) 1994-10-03 2010-10-26 Mars, Incorporated Cocoa extracts as antioxidants
US8460739B2 (en) 2008-01-22 2013-06-11 Barry Callebaut Ag Process for making red or purple cocoa material
CN108164530A (en) * 2018-01-24 2018-06-15 安徽省百花香料香精有限公司 A kind of environmentally friendly process for purification of theobromine
CN114478530A (en) * 2022-02-25 2022-05-13 陕西嘉禾药业有限公司 Method for extracting high-content theobromine from cocoa beans

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7820713B2 (en) 1994-10-03 2010-10-26 Mars, Incorporated Cocoa extracts as antioxidants
US7368144B2 (en) 2000-08-11 2008-05-06 Barry Callebaut France Method for obtaining cocoa bean polyphenol extracts, resulting extracts and uses thereof
US8460739B2 (en) 2008-01-22 2013-06-11 Barry Callebaut Ag Process for making red or purple cocoa material
US9107430B2 (en) 2008-01-22 2015-08-18 Barry Callebaut Ag Process for producing red or purple cocoa-derived material
CN108164530A (en) * 2018-01-24 2018-06-15 安徽省百花香料香精有限公司 A kind of environmentally friendly process for purification of theobromine
CN114478530A (en) * 2022-02-25 2022-05-13 陕西嘉禾药业有限公司 Method for extracting high-content theobromine from cocoa beans
CN114478530B (en) * 2022-02-25 2023-09-19 陕西嘉禾药业有限公司 Method for extracting high-content theobromine from cocoa beans

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