GB821103A - Improvements in or relating to substituted phenyl ureas and herbicidal compositions - Google Patents

Improvements in or relating to substituted phenyl ureas and herbicidal compositions

Info

Publication number
GB821103A
GB821103A GB12905/56A GB1290556A GB821103A GB 821103 A GB821103 A GB 821103A GB 12905/56 A GB12905/56 A GB 12905/56A GB 1290556 A GB1290556 A GB 1290556A GB 821103 A GB821103 A GB 821103A
Authority
GB
United Kingdom
Prior art keywords
hydroxyethyl
methylurea
butyl
oil
water
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
GB12905/56A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB821103A publication Critical patent/GB821103A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C273/00Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C273/18Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
    • C07C273/1809Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety
    • C07C273/1818Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety from -N=C=O and XNR'R"
    • C07C273/1827X being H

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises substituted ureas represented by the formula <FORM:0821103/IV (a)/1> wherein R represents an alkyl group containing 2, 3 or 4 carbon atoms, i.e. an ethyl, propyl, isopropyl, n-butyl, sec.-butyl or tert.-butyl group. The above substituted ureas are obtained by the reaction of appropriately p-alkyl-substituted phenyl isocyanates with methylethanolamine, e.g. in an inert liquid reaction medium such as xylene, toluene or dioxane. In examples: 3 - (p - cumenyl) - 1 - (2 - hydroxyethyl) - 1 - methylurea is obtained by heating p-cumidine with phosgene in xylene solution to reflux temperature until revolution of hydrogen chloride ceases, adding methylethanolamine to the cooled solution and heating and cooling the mixture (I); and other compounds of the above general formula wherein R is ethyl, n-propyl, isobutyl, sec.-butyl and tert.-butyl are similarly prepared (III, V, VII, IX and XI). White solids separate when the isocyanate solutions are first mixed with the methylethanolamine. The substituted ureas are employed in herbicidal compositions (see Group VI).ALSO:A herbicidal composition comprises one or more compounds of the general formula <FORM:0821103/VI/1> wherein R represents an alkyl group containing 2, 3 or 4 carbon atoms (see Group IV (b)) together with a carrier or diluent, said compound or compounds being present in the said composition in an amount sufficient to exert a herbicidal effect. Carriers mentioned include finely-divided solids such as talcs, clays, pyrophyllite, diatomaceous earth and walnut shell, wheat, redwood, soya bean, and cottonseed flours, and liquids, e.g. alkylated naphthalenes and cresols. The ureas may also be employed as dispersions, e.g. in oil and water, and surface-active agents may be included in the powder or liquid compositions. The surface-active agents may be of the anionic, cationic or nonionic types and include sodium and potassium oleates, amine salts of oleic acid such as morpholine and dimethylamine oleates, sulphonated animal and vegetable oils such as sulphonated fish and castor oils, sulphonated petroleum oils, sulphonated acyclic hydrocarbons, the sodium salt of lignosulphonic acid and other surface-active agents listed in "Soap and Sanitary Chemicals" August, September and October, 1949. Fertilizers, other herbicidal agents, insecticides and fungicides may also be included in the compositions. In examples: a powder suitable for dispersion in water for spraying comprises 3-(p-cumenyl) - 1 - (2 - hydroxyethyl) - 1 - methylurea, fuller's earth, sodium lauryl sulphate and methyl cellulose (II); a dusting powder comprises 3-(p-ethylphenyl)-1-(2-hydroxyethyl)-1-methylurea and talc (IV); a powder for spraying in oil, water or a mixture of oil and water comprises 1-(2-hydroxyethyl)-1-methyl-3-(p-n-propylphenyl)-urea, an alkylated aryl polyether alcohol and fuller's earth is dispersed in alkylated naphthalene oil (VI); a composition comprising 3-(p-isobutyl-phenyl)-1-(2-hydroxyethyl)-1-methylurea, a long-chain fatty alcohol sulphate, the sodium salt of lignosulphonic acid and kerosene is dispersed in water (VIII); pellets are prepared from an aqueous mixture of 3 - (p - sec. - butylphenyl) - 1 - (2 - hydroxyethyl) - 1 - methylurea sodium sulphate, the sodium salt of isopropyl naphthalene sulphonate and bentonite (X); and a dusting powder comprises 3 - (p - tert. - butylphenyl) - 1 - (2 - hydroxyethyl)-1-methylurea, cottonseed oil and walnut shell flour.
GB12905/56A 1955-05-02 1956-04-26 Improvements in or relating to substituted phenyl ureas and herbicidal compositions Expired GB821103A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US821103XA 1955-05-02 1955-05-02

Publications (1)

Publication Number Publication Date
GB821103A true GB821103A (en) 1959-09-30

Family

ID=22169120

Family Applications (1)

Application Number Title Priority Date Filing Date
GB12905/56A Expired GB821103A (en) 1955-05-02 1956-04-26 Improvements in or relating to substituted phenyl ureas and herbicidal compositions

Country Status (4)

Country Link
BE (1) BE564322A (en)
FR (1) FR1205117A (en)
GB (1) GB821103A (en)
MY (1) MY6000041A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3779738A (en) * 1969-10-27 1973-12-18 Perro Soc Dev La Vente De Spec Herbicidal para-tert-butylphenyl urea
CN108102087A (en) * 2017-12-25 2018-06-01 湖南华腾制药有限公司 A kind of PEGylated diuron synthesis and its application in weeding
CN108164691A (en) * 2017-12-25 2018-06-15 湖南华腾制药有限公司 A kind of PEGylated substitute urea compound and its application in herbicide

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3779738A (en) * 1969-10-27 1973-12-18 Perro Soc Dev La Vente De Spec Herbicidal para-tert-butylphenyl urea
CN108102087A (en) * 2017-12-25 2018-06-01 湖南华腾制药有限公司 A kind of PEGylated diuron synthesis and its application in weeding
CN108164691A (en) * 2017-12-25 2018-06-15 湖南华腾制药有限公司 A kind of PEGylated substitute urea compound and its application in herbicide
CN108102087B (en) * 2017-12-25 2021-01-05 湖南华腾制药有限公司 Synthesis of PEG (polyethylene glycol) diuron and application of PEG diuron in weeding

Also Published As

Publication number Publication date
BE564322A (en)
MY6000041A (en) 1960-12-31
FR1205117A (en) 1960-01-29

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