GB1110819A - N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production - Google Patents

N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production

Info

Publication number
GB1110819A
GB1110819A GB5492666A GB5492666A GB1110819A GB 1110819 A GB1110819 A GB 1110819A GB 5492666 A GB5492666 A GB 5492666A GB 5492666 A GB5492666 A GB 5492666A GB 1110819 A GB1110819 A GB 1110819A
Authority
GB
United Kingdom
Prior art keywords
trifluoromethyl
dinitroaniline
hydroxypropyl
formula
compounds
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
GB5492666A
Inventor
Keiichi Maruo
Hiroshi Ono
Tatsumasa Shimoike
Toshikazu Higuchi
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.)
Daikin Industries Ltd
Original Assignee
Daikin Industries Ltd
Daikin Kogyo Co 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 Daikin Industries Ltd, Daikin Kogyo Co Ltd filed Critical Daikin Industries Ltd
Priority to GB5492666A priority Critical patent/GB1110819A/en
Publication of GB1110819A publication Critical patent/GB1110819A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
    • C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
    • C07C215/16—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to carbon atoms of six-membered aromatic rings

Abstract

The invention comprises compounds of the formula <FORM:1110819/C2/1> in which R and R1 are each a hydroxy alkyl group containing 1-5 carbon atoms. They are prepared by heating a compound of formula <FORM:1110819/C2/2> in which X is a halogen atom with a compound of formula HNRR1. Among the new compounds prepared by the process are N,N-di(2-hydroxyethyl) - 2 - trifluoromethyl - 4,6 - dinitroaniline; N,N - di - (3 - hydroxypropyl) - 2- trifluoromethyl - 4,6 - dinitroaniline; N,N - di - (2-hydroxypropyl) - 2 - trifluoromethyl - 4,6 - dinitroaniline; N - (2 - hydroxyethyl) - N - (3-hydroxypropyl) - 2 - trifluoromethyl - 4,6 - dinitroaniline; and N - (2 - hydroxyethyl) - N (2 - hydroxypropyl) - 2 - trifluoromethyl - 4,6-dinitroaniline.ALSO:Compounds of the formula <FORM:1110819/A5-A6/1> in which R and R1 are each hydroxy alkyl groups having 1-5 carbon atoms are used as active agents in herbicidal compositions. The compounds may be used alone or in admixture with standard carrier materials or conditioning agents. They may be mixed with suitable inert solids, e.g. natural clays, diatomaceous earth, walnut shell flour, wood flour, synthetic silica and calcium silicate, and used as dusts. They may be made into liquid preparations by dissolving or suspending in, e.g. kerosene, Stoddard solvent, xylene, alcohols, alkylated napthalene, glycols and ketones. They may also be used in the form of wettable powders and these and the liquid compositions may also contain dispersing or emulsifying agents.
GB5492666A 1966-12-08 1966-12-08 N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production Expired GB1110819A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5492666A GB1110819A (en) 1966-12-08 1966-12-08 N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5492666A GB1110819A (en) 1966-12-08 1966-12-08 N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production

Publications (1)

Publication Number Publication Date
GB1110819A true GB1110819A (en) 1968-04-24

Family

ID=10472477

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5492666A Expired GB1110819A (en) 1966-12-08 1966-12-08 N,n-di(hydroxyalkyl)-2-trifluoromethyl-4,6-dinitroanilines and their production

Country Status (1)

Country Link
GB (1) GB1110819A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3764625A (en) * 1969-04-01 1973-10-09 United States Borax Chem Trifluoromethyl-1,3-phenylenediamine compounds
US3764623A (en) * 1969-04-01 1973-10-09 United States Borax Chem Herbicidal dinitro-1,3-phenylenediamine compounds
WO2006108224A1 (en) * 2005-04-11 2006-10-19 Murdoch University Antiparasitic compounds

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3764625A (en) * 1969-04-01 1973-10-09 United States Borax Chem Trifluoromethyl-1,3-phenylenediamine compounds
US3764623A (en) * 1969-04-01 1973-10-09 United States Borax Chem Herbicidal dinitro-1,3-phenylenediamine compounds
WO2006108224A1 (en) * 2005-04-11 2006-10-19 Murdoch University Antiparasitic compounds

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