GB336111A - Improvements in the manufacture and production of thiourea - Google Patents
Improvements in the manufacture and production of thioureaInfo
- Publication number
- GB336111A GB336111A GB3182429A GB3182429A GB336111A GB 336111 A GB336111 A GB 336111A GB 3182429 A GB3182429 A GB 3182429A GB 3182429 A GB3182429 A GB 3182429A GB 336111 A GB336111 A GB 336111A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohols
- liquids
- thiourea
- mixtures
- hydrogen sulphide
- 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
Links
Landscapes
- Extraction Or Liquid Replacement (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
336,111. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Oct. 19, 1929. Thiourea is produced by treating calcium cyanamide with hydrogen sulphide in the absence of liquids or in the, presence of small quantities of liquid sufficient to give a paste. The thiourea i.s extracted from the reaction mixture by means of organic solvents. In forming the paste, there may be used water or aqueous liquids, or organic liquids capable of dissolving hydrogen sulphide, such as alcohols, e.g. methyl and ethyl alcohols, or amines, e.g. aniline and alkylamines, or esters, e.g. ethyl acetate, or pyridine, or hydrocarbons and their halogen derivatives, e.g. benzene or mixtures of organic liquids may be used during the conversion. In some cases it is advantageous to add alkaline substances such as ammonia and gaseous amines to the liquids. Frequentlythe hydrogen sulphide is caused to react at high pressures and while stirring. The temperature should not normally exceed 100‹ C. For the extraction, liquids are chosen which dissolve the thiourea but not the lime compounds, as for example ketones, e.g. acetone, also pyridine and its homologues, but especially mixtures of organic liquids such as mixtures of alcohols and ethers, or of alcohols and benzene, or of alcohols and chloroform, carbon tetrachloride, or benzene, and in some cases mixtures of organic liquids with water, e.g. aqueous alcohols. When water is present during the reaction it is often advantageous to dry the mass resulting from the reaction before the extraction. It is preferable to extract with hot solvents; the thiourea may then be recovered by cooling, and the mother liquor used again for extraction. The thiourea may also be obtained by evaporation of the solvent. In the examples, a paste is made with ethyl alcohol or aqueous ammonia, or the cyanamide is treated with gaseous ammonia before the introduction of hydrogen sulphide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3182429A GB336111A (en) | 1929-10-19 | 1929-10-19 | Improvements in the manufacture and production of thiourea |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3182429A GB336111A (en) | 1929-10-19 | 1929-10-19 | Improvements in the manufacture and production of thiourea |
Publications (1)
Publication Number | Publication Date |
---|---|
GB336111A true GB336111A (en) | 1930-10-09 |
Family
ID=10328954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3182429A Expired GB336111A (en) | 1929-10-19 | 1929-10-19 | Improvements in the manufacture and production of thiourea |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB336111A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2498782A (en) * | 1942-05-13 | 1950-02-28 | Rhone Poulenc Sa | Preparation of aryl sulfonyl thioureas |
US2521778A (en) * | 1946-11-04 | 1950-09-12 | Saint Gobain | Preparation of thiourea |
US2545764A (en) * | 1943-10-19 | 1951-03-20 | Rhone Poulenc Sa | Preparation of sulfanilylthiourea |
US2547147A (en) * | 1944-11-29 | 1951-04-03 | Monsanto Chemicals | Method of producing sulfanilylthioureas |
CN102731356A (en) * | 2011-04-15 | 2012-10-17 | 中国石油化工股份有限公司 | Thiourea cleaning production method |
CN114644582A (en) * | 2022-04-11 | 2022-06-21 | 中原工学院 | Preparation method of phenyl bis-thiourea compound |
-
1929
- 1929-10-19 GB GB3182429A patent/GB336111A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2498782A (en) * | 1942-05-13 | 1950-02-28 | Rhone Poulenc Sa | Preparation of aryl sulfonyl thioureas |
US2545764A (en) * | 1943-10-19 | 1951-03-20 | Rhone Poulenc Sa | Preparation of sulfanilylthiourea |
US2547147A (en) * | 1944-11-29 | 1951-04-03 | Monsanto Chemicals | Method of producing sulfanilylthioureas |
US2521778A (en) * | 1946-11-04 | 1950-09-12 | Saint Gobain | Preparation of thiourea |
CN102731356A (en) * | 2011-04-15 | 2012-10-17 | 中国石油化工股份有限公司 | Thiourea cleaning production method |
CN114644582A (en) * | 2022-04-11 | 2022-06-21 | 中原工学院 | Preparation method of phenyl bis-thiourea compound |
CN114644582B (en) * | 2022-04-11 | 2024-03-29 | 中原工学院 | Preparation method of phenyl dithiourea compound |
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