GB190610228A - Improvements in the Manufacture and Production of Polychloramidines and Alkylderivatives thereof - Google Patents

Improvements in the Manufacture and Production of Polychloramidines and Alkylderivatives thereof

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Publication number
GB190610228A
GB190610228A GB190610228DA GB190610228A GB 190610228 A GB190610228 A GB 190610228A GB 190610228D A GB190610228D A GB 190610228DA GB 190610228 A GB190610228 A GB 190610228A
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United Kingdom
Prior art keywords
amidines
nitro
compounds
trichlorbenzene
nitroalkylacylamino
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
Inventor
James Yate Johnson
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Application granted granted Critical
Publication of GB190610228A publication Critical patent/GB190610228A/en
Expired legal-status Critical Current

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Abstract

10,228. Johnson, J. Y., [Badische Anilin & Soda Fabrik]. May 1. Chlorbenzimidazoles.-Relates to the production of amidines of the general formulawhere R represents hydrogen, alkyl, or aryl, and gamma represents hydrogen or chlorine. The amidines derived from as-trichlordiaminobenzene and v-tetrachlordiaminobenzene are particularly useful. The amidines are produced by reducing the o-nitroacylamino. or o-nitroalkylacylamino-derivatives of tri- or tetra-chlorbenzene. A mixture of the amidine and diamino compounds is usually obtained. The diamino compounds with or without previous separation are converted into the amidines by heating either alone or with a dehydrating- agent. The amidines obtained from non-alkylnitroacylamino compounds may be converted into alkylated derivatives isomeric with those obtained from the nitroalkylacylamino compounds, by treating tbeir alkali compounds with an agent such as methyl chloride. The following are suitable parent materials for use in the above process: 1-formyl- or acetyl-amino-2-nitro-3 : 4 : 6-trichlorbenzene (obtained by nitrating formyl-or acetyl-trichloranilide), 1-methylformylamino-2-nitro-3 : 4 : 6-trichlorbenzene, 1-ethylacetylamino-2-nitro-3 : 4 : 6-trichlorbenzene, and 1-ethyl- or benzyl-acetylamino- or benzoylamino-2-nitro 3 : 4 : 5 : 6-tetrachlorbenzene.
GB190610228D 1906-05-01 1906-05-01 Improvements in the Manufacture and Production of Polychloramidines and Alkylderivatives thereof Expired GB190610228A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB190610228T 1906-05-01

Publications (1)

Publication Number Publication Date
GB190610228A true GB190610228A (en) 1906-07-26

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ID=32433634

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Application Number Title Priority Date Filing Date
GB190610228D Expired GB190610228A (en) 1906-05-01 1906-05-01 Improvements in the Manufacture and Production of Polychloramidines and Alkylderivatives thereof

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GB (1) GB190610228A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2876230A (en) * 1956-11-23 1959-03-03 Merck & Co Inc 1-halomercuri, trihalo benzimidazoles

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2876230A (en) * 1956-11-23 1959-03-03 Merck & Co Inc 1-halomercuri, trihalo benzimidazoles

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