GB371555A - An improved process for the manufacture of acetamide and acetic acid - Google Patents

An improved process for the manufacture of acetamide and acetic acid

Info

Publication number
GB371555A
GB371555A GB8371/31A GB837131A GB371555A GB 371555 A GB371555 A GB 371555A GB 8371/31 A GB8371/31 A GB 8371/31A GB 837131 A GB837131 A GB 837131A GB 371555 A GB371555 A GB 371555A
Authority
GB
United Kingdom
Prior art keywords
formamide
hydrogen
acetamide
mixture
ammonia
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
GB8371/31A
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.)
FR DE CATALYSE GENERALISEE SOC
Original Assignee
FR DE CATALYSE GENERALISEE SOC
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 FR DE CATALYSE GENERALISEE SOC filed Critical FR DE CATALYSE GENERALISEE SOC
Publication of GB371555A publication Critical patent/GB371555A/en
Expired legal-status Critical Current

Links

Abstract

Acetamide is obtained by causing hydrogen to react on formamide, or on a mixture of carbon monoxide and ammonia, under the influence of ultra-violet or infra-red radiations. The reaction between hydrogen and formamide takes place at ordinary pressure and at temperatures between 200 and 500 DEG C. When carbon monoxide and ammonia are used, pressures of at least 100 kg. per sq. cm. and temperatures between 100 and 300 DEG C. are employed. Catalysts consisting of pumicestone, carbon powder, finely divided metals, particularly copper, or metal oxides such as aluminium oxide may be present. According to an example, formamide vapour mixed with hydrogen is passed at 250-300 DEG C. through a quartz tube containing pumicestone, carbon powder, copper powder, aluminium oxide, or a mixture of the two latter substances, under the influence of ultra-violet light from mercury vapour lamps. By cooling the exit gases, acetamide is obtained. The Specification as open to inspection under Sect. 91 (3) (a) describes also the production of di- and tri-acetamide and of glycocoll by the reaction referred to above. This subject-matter does not appear in the Specification as accepted.ALSO:Acetamide, which may subsequently be converted to acetic acid by hydrolysis, is obtained by causing hydrogen to react on formamide, or on a mixture of carbon monoxide and ammonia. The reaction between hydrogen and formamide may take place at ordinary-pressure and at a temperature between 200 and 500 DEG C. When carbon monoxide and ammonia are substituted for formamide, pressures of at least 100 Kg. per sq. cm. and temperatures between 100 and 300 DEG C. are employed. Both reactions are facilitated by the presence of catalysts consisting of pumicestone, carbon powder, finely divided metals, particularly copper, or metal oxides such as aluminium oxide, and by the influence of ultra-violet or infra-red radiations. According to examples, (1) formamide vapour mixed with hydrogen is passed at 250-300 DEG C. through a quartz tube containing pumicestone, carbon powder, copper powder, aluminium oxide, or a mixture of the two latter substances, under the influence of ultra-violet light from mercury vapour lamps. By cooling the exit gases, acetamide is obtained, which is hydrolysed in known manner to acetic acid; steam may be added to the initial mixture to facilitate the reaction; and (2) a mixture of carbon monoxide and hydrogen obtained, for example, by passing steam over red-hot carbon, is passed together with ammonia under a pressure of 100 Kg. per cm., and at 250-300 DEG C. over the same catalysts as in (1) above, the acetamide obtained being hydrolysed to acetic acid as before. The Specification as open to inspection under Sect. 91 (3) (a) refers also to the production of di- and triacetamide and of glycocoll by the action of hydrogen on formamide. This subject-matter does not appear in the Specification as accepted.
GB8371/31A 1930-03-26 1931-03-18 An improved process for the manufacture of acetamide and acetic acid Expired GB371555A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR371555X 1930-03-26

Publications (1)

Publication Number Publication Date
GB371555A true GB371555A (en) 1932-04-28

Family

ID=8894706

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8371/31A Expired GB371555A (en) 1930-03-26 1931-03-18 An improved process for the manufacture of acetamide and acetic acid

Country Status (1)

Country Link
GB (1) GB371555A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571911A (en) * 1949-11-19 1951-10-16 American Cyanamid Co Preparation of guanidine salts
US4244889A (en) 1979-12-19 1981-01-13 Union Carbide Corporation Production of acetamides with rhodium-manganese catalysts
US4556734A (en) * 1983-11-04 1985-12-03 Texaco Inc. Process for synthesizing formamides from synthesis gas plus ammonia

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571911A (en) * 1949-11-19 1951-10-16 American Cyanamid Co Preparation of guanidine salts
US4244889A (en) 1979-12-19 1981-01-13 Union Carbide Corporation Production of acetamides with rhodium-manganese catalysts
US4556734A (en) * 1983-11-04 1985-12-03 Texaco Inc. Process for synthesizing formamides from synthesis gas plus ammonia

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