US3349115A

US3349115A - Sulfur-containing carbamate insecticides

Info

Publication number: US3349115A
Application number: US259755A
Authority: US
Inventors: Edward D Weil; Hans L Schlichting
Original assignee: Hooker Chemical Corp
Current assignee: Occidental Chemical Corp
Priority date: 1963-02-19
Filing date: 1963-02-19
Publication date: 1967-10-24
Anticipated expiration: 1984-10-24

Description

3,349,115 Patented Get. 24, 1967 [ice 3,349,115 SULFUR-CGNTAINlNG CARBAMATE INSECTECKDES Edward D. Weil, Lewiston, and Hans L. Schlichting,

Grand island, N.Y., assignors to Hooker Chemical Corporation, Niagara Fails, N.Y., a corporation of New York No Drawing. Filed Feb. 19, 1963, Ser. No. 259,755 8 Claims. (Cl. 260-479) This invention relates to new and useful insecticidal compounds. These compounds may be described by the general formula:

wherein Y is a divalent lower alkylene radical, or two monovalent radicals R and R R and R are alkyl groups of up to 6 carbon atoms, substituted alkyl of up to 6 carbon atoms, phenyl, lower alkylphenyl, benzyl, lower alkylbenzyl, halophenyl, and halobenzyl substituents; R R and R are hydrogen, lo-wer alkoxy, or lower alkyl substituents; R is a hydrogen or lower alkyl substituent; and R is a lower alkyl substituent.

Thus embraced within the present generic invention are the subgeneric compositions:

R R o C ONR CON S SR R on Grim and R -03 s X SR2 R R R R wherein the R groups are as previously defined and n is a number from one to four.

By the term substituted as applied tolower alkyl is meant substituted by a vinyl, lower alkoxy, chlorine, carboalkoxy, or hydroxy substituent.

The term lower as applied to alkyl or alkylene groups in the present application means such a group containing up to four carbon atoms.

The a t-bis(alkylmercapto)methyl group may be in the ortho, meta, or para position with respect to the carbamate group on the central ring. R R and R may then be substituted on open positions of the ring to form a total of four substituents thereupon, not including the carbamate, only one of the four other than hydrogen, allowed to be in an ortho position with respect to the carbamate group.

Examples of compounds included within the scope of the invention are the N-methylcarbamates and N,N- dimethylcarbamates of the following salicylaldehyde mercaptals: dimethyl mercaptal, diethyl mercaptal, dipropyl mercaptal, diisopropyl mercaptal, di-n-butyl mercaptal, diisobutyl mercaptal, di-sec-butyl mercaptal, diamyl mercaptal, dihexyl mercaptal, dicyclohexyl mercaptal, diallyl mercaptal, diphenyl mercaptal, ditolyl mercaptal, dixylyl mercaptal, di(p-chlorophenyl) mercaptal, dibenzyl mercaptal, di-p-chlorobenzyl mercaptal, and di-2,5-dichlorobenzyl mercaptal; also the N-methylcarbamates and N,N- dimethylcarbamates of the cyclic mercaptals from salicylaldehyde and ethane-1,2-dithio, propane-1,2-dithiol, propane-1,3-dithiol, butane-1,2-dithiol, butane-1,3-dithiol, and

butane-1,4-dithiol, for example. Also included within the scope of the invention are the corresponding mercaptals from 3, 4, or 5-methyl-, isopropyl-, or sec-butylsalicylaldehyde such as the N-methylcarbamate of 3, 4, or 5- methylsalicylaldehyde dimethyl mercaptal, 3, 4, or 5- isopropylsalicylaldehyde diethyl mercaptal, and 3, 4, or 5-sec-butylsalicylaldehyde cyclic mercaptal from ethanel,2-dithiol. Also included are such compounds as the following: the N-methylcarbamate of 3,5-dimethyl salicylaldehycle dimethyl mercaptal, the N-methylcarbamate of 3,5-dirnethyl salicylaldehyde cyclic mercaptal from ethane- 1,2-dithiol, the N-methylcarbamate of 3,5-diisopropylsalicylaldehyde dimethyl mercaptal, and the N-methylcarbamate of 3,5-dimethyl-4-isopropylsalicylaldehyde dimethyl mercaptal.

It is preferred in the present invention that R and R be the same when alkyl, and it is further preferred that they be methyl groups; when conjoined, an ethylene group bridging the two sulfur atoms is preferred. R R and R are preferably hydrogen, but When they are lower alkyl, methyl is preferred; when they are lower alkoxy, up to three carbon atoms in the group is preferred and still more preferred is a methoxy substituent. When R R and R are halophenyl or halobenzyl, chloro-substituted compounds are preferred, although bromo compounds are also useful. R and R may both be alkyl groups, preferably containing not more than three carbon atoms, and more preferably are both methyl. Still more preferred is for R to be hydrogen, and R to be a lower alkyl, preferably containing not more than three carbon atoms, and more preferably it is a methyl substituent.

Because of exceptional activity, the most preferred embodiments of the invention are:

?OONHCH OCONHCHZ 86113 s-on,'

S-CH:

sons and In general the compounds of the invention may be prepared by reacting aldehydes of the structure:

CH=O

' the carbamate. The first reaction proceeds best in the presence of a strong acid catalyst such as hydrogen chlo ride, sulfuric acid, toluenesulfonic acid, or the like, and may be conducted with the aldehyde in the liquid phase at any temperature between about -30 to +200 C. Sol vents are not necessary but may be employed. Suitable solvents are, for example, hydrocarbons such as petroleum ether, benzene, toluene, or the like, ethers such as ethyl ether, or any other solvent inert to aldehydes, to thiols, and to strong acids. The reaction proceeds with the evolution of water, which usually separates out as a different phase from the intermediate product. The conversion of the resultant phenol to the carbamate may be conducted by addition of at least one molar equivalent of a lower alkyl isocyanate, methyl isocyanate, conveniently in the presence of a catalyst such as a strong tertiary amine or an organotin salt, or by addition of at least one molar equivalent of a lower alkyl or dialkyl carbamyl chloride in the presence of one molar equivalent of an acceptor for hydrogen chloride, such as a tertiary base, or by reaction of the phenol with phosgene to obtain the themselves as insecticides and as. nematocides, but have further utility as intermediates in the oxidation (with H thereof to compounds of the formula:

Ra OCON where n is one or two, and the R groups are as previously defined.

Such oxidized. compounds, sulfoxides and sulfones, are water soluble, whereas the parent sulfide compounds are not, and as suchare preferred for use in plant systems where they are not toxic to the plant but are toxic to plant-eating pests. The present compositions may be used as such, or more generally, formulated with various adjuvants. For example, they may be used as a reaction crude or as the crystalline product, or may be employed by mixing it with conventional pest control adjuvants, diluents or conditioning agents, which act as inert carriers, to provide compositions in the form of solutions, emulsions, dispersions, powders dispersible in wateror other solvents, dusts or the like. For example, it may be formulated with a carrier or diluent substance such as finely divided solid, a solvent of organic or inorganic origin, water, a surface active agent or aqueous emulsion or any suitable combination of one or more of any of these. For household and barn use, formulations with aerosol propellants such as the Freons are convenient. Such formulations or compositions facilitate handling and application and frequently enhance insecticidal elfectiveness.

The liquid compositions discussed generally above, whether solutions or dispersions of the active agents in a liquid solvent or a wettable powder, may contain conditioning agents such as wetting agents, dispersing agents, emulsifying agents, suspending agents and the like known generally as surface active agents. A suitable but not ex haustive listing of these surface active agents are set forth among other places in Soap and Chemical Specialties, vol. 31, No. 7, pages 50-61; No. 8, pages 48-61; No. 9, pages 52-67 and No. 10, pages 38-67 (1955).

Since the exact amount of insecticide in a given mixture will depend upon the type of use, species of insect, mode of formulation, mode of application, prevailing atmospheric conditions and other variables, it is not possible to state this application rate, generally with any degree of preciseness. However, where the insecticide is made up to treat crops being attacked by an insect pest, the general application rate of active insecticide will range from 0.03- pounds per acre with the upper rates above this figure limited by economics. In application to dwelling places and barns, a deposit of at least one mg. per square foot of surface is preferred. It maybe said in passing that a diluent, conditioning agent and/ or adjuvant material will usually make up the bulk of the insecticidal compositions with the active ingredient ordinarily being present on a percent weight basis of under ten percent, but generally, above 0.005 percent.

The insecticide of the invention is compatible with other insecticides and may be used in combination with of America, vol. 6, No. 2, pp. 56-72 (1960), said insecticides acting to complement, supplement, synergisc, or otherwise enhance the activity of the insecticide of the invention. Since an outstanding merit of the present invention is low toxicity, it is preferred to combine applicants new compound with other insecticides and activators of low toxicity, for example, DDT, DDD, methoxychlor, isobornyl thiocyanoacetate, lauryl thiocyanate, lethanes (substituted alkyl thiocyanates), malathion, ronnel, pyrethrins, synthetic. pyrethrin analogs, 0,0 ,limethyl 2,2-dichlorovinyl phosphate, phosdrin, lindane, toxaphene, and the like. Since the compound of this invention has relatively low miticidal activity, it is advantageous to combine it with a miticide such as 1,1-bis(pchlorophenyl)-2,2,2-trichloroethanol, p-chlorophenyl 2,4, 5-trichlorophenyl sulfone, aryl alkyl sulfites, ethion, dimethoate, phorate, demeton, phosphamidon, quinoxaline trithiocarbanates, zineb, sulfur and bis(pentachlorocyclopentadienyl). The compound of the invention, because of its fast action, is useful in combination with slow-acting ingestion insecticides such as the product of melting point one hundred and forty-eight degrees from hexachlorocyclopentadiene and chlorosulfonic acid as de scribed in US. Patent 2,516,404 (1951).

The insecticide of the invention may also be synergised by insecticidal synergists such as the following examples:

Piperonyl. butoxide Sesoxane(2-(3,4-methylenedioxyphenoxy) 3,6,9 trioxaundecane) Sulfoxide n-octyl sulfoxide of isosafrole) n-propyl isome Sesamine oil extractives Octachlorodipropyl ether Other synergists usable with the compound of the invention are those listed by Kenaga, loc. cit., pp. 55-56.

When combined with other active materials, it frequently is convenient to use inert solid carriers or diluents.

Example 1 Into a mixture of 9.4 parts of ethane-1,2-dithiol, 12.2 parts of salicylaldehyde, and 50 parts of benzene was passed a stream of hydrogen chloride gas until an exothermic reaction ensued. The hydrogen chloride stream was then stopped. After an hour, the solution was washed.

with aqueous sodium bicarbonate, then was dried over magnesium sulfate, filtered to remove the drying agent, and the benzene was removed by distillation, leaving the product as a pale tan-colored oil.

Analysis.-Calculated for C H OS neutralization equivalent, 198. Found: neutralization equivalent, 194.

To a solution of 5.9 parts of the above phenol in parts of benzene were added 2.04 parts of methyl isocyanate and 0.05 part of dibutyltin dilaurate (catalyst). When the resultant exothermic reaction subsided, the mixture was briefly warmed to reflux, then was cooled to 20 and the resultant solids were filtered out to obtain 8 parts of colorless crystals, M.P. 142-3 Analysis-Calculated for C H O S N: S, 25.1; N, 5.49. Found: S, 24.5; N, 5.67.

Example 2 A solution of 9.2 parts of salicylaldehyde, 8.1 parts of 1,3 propanedithiol, 0.1 part of p toluenesulfonic acid, and 45 parts of benzene was refluxed 4 hours, then cooled and filtered. The filtrate was washed with aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and the benzene was evaporated. The product was recrystallized from benzene-heptane mixture to obtain 6 parts of light yellow crystals, M.P. 90 (decomposes).

This product was dissolved in 30 parts of benzene and 2 parts of methyl isocyanate added, as Well as 0.05 part dibutyltin dilaurate catalyst. After the exotherm subsided, the solution was briefly refluxed, the two volumes of heptane added, and chilled. There was obtained, upon filtration, 5.5 parts of colorless crystals.

Analysis.Calculated for C H O S N: N, Found: N, 5.3.

Example 3 Into a solution of 12.2 parts of salicylaldehyde, 13.6 parts of ethyl mercaptan, and 100 parts benzene, a stream of hydrogen chloride was passed for one-half hour. After four days, the solution was washed with aqueous sodium bicarbonate, then stripped to a boiling point of 100 at 0.2 mm. in a short-path still. The residual liquid was found by infrared analysis to have a phenolic OH group and no carbonyl.

Analysis.Calculated for C H OS S, 28.1. Found: S, 27.5.

A solution of 4.6 parts of this phenol, 1.5 parts of methyl isocyanate, 20 parts of benzene, and 0.01 part of Dabco (a commercial ditertiary diamine) was refluxed gently for 1 hour, then stripped to a pot temperature of 100 mm.) to leave the product as a syrup. Infrared analysis confirmed the presence of the carbamate structure and the absence of the OH group.

Analysis.Calculated for C H O NS N, 4.9. Found: N, 4.5.

Example 4 Example 5 A solution of 10.6 parts of salicylaldehyde, 24.8 parts of benzyl mercaptan, and 90 parts of benzene was treated with dry HCl and let stand four days, then was stripped to 100 (0.2 mm. Hg pressure), leaving a waxy solid residue, shown by infrared analysis to be a phenolic free of carbonyl groups.

Analysis.--Calculated for C H OS S, 18.17. Found: S, 18.2.

A solution of 6 parts of the above phenol, 1.5 parts of methyl isocyanate, 16 parts of benzene, and 0.02 part of dibutyltin dilaurate was gently refluxed for one hour. Then two volumes of heptane were added and the solution was partly evaporated at room temperature under vacuum until crystallization occurred. The crystals were isolated by filtration and amounted to 4 parts of colorless solid, M.P. 102-1025 C.

Analysis.Calculated for C H O NS Found: N, 3.41.

Example 6 A solution of 10.6 parts of salicylaldehyde and 22 parts of thiophenol in 90 parts of benzene was treated with hydrogen chloride as above. Upon stripping the product to 100 (0.2 mm. Hg pressure), there remained a viscous phenolic oil free of aldehyde groups.

less crystals, M.P. -100.5 C.

Analysis.--Calculated for C H O NS 3.67.

Found: N, 3.53.

Example 7 Into a solution of 21 parts of salicylaldehyde in 50 parts of benzene was passed a stream of methyl mercaptan which was first passed through a vessel containing strong hydrochloric acid to entrain a catalytic amount of hydrogen chloride. The reaction mixture underwent spontaneous heating to 60. After one hour, the mixture was stripped to a temperature of (2.5 mm. Hg pressure), leaving a phenolic oil having no aldehyde group according to infrared analysis.

To 6 parts of this intermediate was added 2 parts of methyl isocyanate in 20 parts of benzene plus 0.05 part of dibutyltin dilaurate catalyst. When the exothermic reaction subsided, the mixture was refluxed for one hour, then stripped free of solvent to leave an oil having the correct analysis for the desired carbamate.

Analysis.-Calculated for C H O S N: N, Found: N, 5.1.

Example 8 An isomer mixture of 3-methyland S-methylsalicylaldehyde (prepared by the Reimer-Tiemann reaction of chloroform with m-cresol) was treated with methyl mercaptan under the conditions of the preceding example and was worked up in the same way to obtain a light brownish oil having a phenolic group and no aldehyde carbonyl group (by infrared analysis).

To 6.5 parts of this phenol in 20 parts of benzene Was added 2 parts of methyl isocyanate, 0.02 part of Dabco catalyst (description given previously) and 0.02 part of dibutyltin dilaurate. The solution was refluxed 2 hours, then was stripped free of solvent to obtain a viscous brownish oil.

Analysis.-Calculated Found: N, 5.0.

for C H O S N: N, 5.2.

Example 9 Following the method of Example 7, 3,5-dimethyl salicylaldehyde was reacted with methyl mercaptan to obtain, on stripping of the solvent, a light brown waxy semisolid which, by infrared analysis, was free of aldehyde groups and contained a phenolic OH. To a solution of 6.5 parts of this intermediate in 25 parts of benzene was added 2 parts of methyl isocyanate, 0.01 part of Dabco, 0.01 part of dibutyltin dilaurate, and the whole was then refluxed for 3 /2 hours. The solvent was stripped to a pot temperature of 100 (12 mm. Hg pressure), leaving a syrup which set to a brownish Waxy solid on standing at room temperature.

Analysis.Calculated for Found: N, 4.7.

Example 10 To a solution of 29 parts of p-chlorothiophenol in 100 parts benzene were added 12 parts of salicylaldehyde and 1 part zinc chloride. After refluxing for 3 hours, the reaction mixture was diluted with ethyl ether, washed with aqueous sodium bicarbonate, dried over calcium chloride, and evaporated to yield 35 parts of salicylaldehyde bis- (p-chlorophenyl mercaptal), M.P. 7677 C.

Analysis.Calculated for C H OS Cl S, 16.29; Cl, 18.07. Found: S, 16.73; Cl, 17.9.-

A solution of 8 parts of this phenol in 50 parts of benzene was treated with 2 parts of methyl isocyanate in the presence of 0.01 part of Dabco (a commercial ditertiary diamine) in the manner as described in Example 3. The

7 residue obtained on evaporating was recrystallized from chloroform to yield 9.4 parts of the desired methylcarbamate, M.P. 159 C.

8 indicated in the following table, onto several species of insects. The percent kill was estimated after twenty-four hours;

Percent Kill (at Concentration Indicated) Chemical Mexican Bean Aphid. Mitesv Bean Beetle N-methylcarbamate ol Salicylaldehyde dimethyl mercaptal 100 (0.1%) 100 (0. 0025%) 100 (0.1%) Salicylaldehyde diethyl mercaptal 40 95 75 Salieylaldehyde diphenyl mercap 50 Salicylaldehyde di-p-ehlorophenyl mercaptal 99 1%) Salicylaldehyde 1,2-ethanedithiol mercaptal 100 100 Salicylaldehytle 1,3-propa11edithiol mercaptal 100 3-; and 5-methylsalicylaldehyde dimethyl mereaptaL. 100 (0. 1%) 100 (0. 1%) 100 (0.1%) 3,fi-dimethylsalicylaldehyde dimethyl mercaptal 100 (0. 1%) 100 (0. 1%) 100 (0. 1%) Salicylaldehyd (0.1%) 30 (0.1%) 0 (0. 1%) p-Hydroxybenzaldehyde 1,2-ethanedithiol mercaptal. 0 (0.1%) 0 (0.1%) 0 (0. 1%)

Analyszs.Calculated for C H O S Cl N, 3.11; Cl, Example 16 15.78; S, 14.22..Found: N, 3.0; Cl, 15.40; S, 13.96.

Example 11 Example 12 An emulsifiable formulation was made up by blending the following:

Product of Example 11 pounds 2 Polyoxyethylene ether-sodium alkylarylsulfonate emulsifier blend do 0.4

Xylene: isophorone 3:1 (volume) blend 0) *To make 1 gallon.

the resultant solution could be emulsified with water in any amount to prepare insecticidal emulsion sprays.

Example 13 A wettable powder formulation was made by grinding together the following ingredients in a hammer mill:

Parts by weight Product of Example 1 50 Lignin sulfonate dispersing agent 6 Sorbit P (arylsulfonate salt-wetting agent) 3 Attapulgus clay 41 The mixture was suspended in water by slight agitation before and during spraying.

Example 14 An insecticidal dust was made by blending the following ingredients:

Parts by weight Product of Example 8 Attapulgus clay Diluex (clay) 85 Example 15 Contact insecticidal activity of representative compounds of the invention was determined by spraying aqueous dispersions of the compounds, at the concentrations Systemic activity of the N-methylcarbamate of salicylaldehyde ethane 1,2-dithiol mercaptal was determined by applying ml. of a 0.1% aqueous dispersion of the compound to the soil in which are planted nasturtiums infested with aphids and bean plants infested with mites. The kill of the aphids and mites was determinedto be 100% at 24 to 48 hours respectively.

Example 17 Nematocidal activity of the N-methylcarbamate of salicylaldehyde ethane-1,2-dithiol mercaptal was determined by admixing the compound at 0.5 g./gallon with soil infested with Meloidogyne incognita. Cucumber seedlings were then planted in the treated soil,and also in some infested but untreated soil for comparison. After 10 days, the cucumber plants were uprooted and 100% repression of root lesions (root knots) was observed relative to the untreated comparison plants.

In the foregoing examples and in the specification and claims, all parts given are by weight and all temperatures are in degree centrigrade, unless otherwise indicated.

The present invention has been described with respect to preferred examples thereof but is not to be interpreted as limited thereto and would be apparent to one of skill in the art that substitutions may be made without departing from the invention.

What is claimed is:

1. New compositions of the formula:

R6 OCON wherein R and R are selected from the group consisting of alkyl of up to 6 carbon atoms, substituted alkyl of up to 6 carbon atoms, wherein said substituent is selected from the group consisting of vinyl, chlorine, hydroxy, phenyl, lower alkylphenyl, benzyl, lower alkylbenzyl, chlorophenyl, cyclohexyl and chlorobenzyl, R R and R are selected from the group consisting of hydrogen, chlorophenyl, bromophenyl, chlorobenzyl, bromobenzyl,

lower alkyland lower alkoxy, with only one of the groups of 9 and R R and R other than hydrogen, being allowed to be ortho to the R O C ON carbamate group, R is selected from the group consisting of hydrogen and a lower alkyl, and R is a lower alkyl.

2. The composition of claim 1 in which R and R a ethyl.

3 The composition of claim 1 in which R and R are methyl.

4. The composition of claim 3 in which R R and R are methyl.

5. The composition of claim 1 in which R R and R are lower alkyl.

6. The composition of claim 3 in which R R and R are hydrogen and R is hydrogen and R is lower alkyl.

7. The composition:

OOONHCH3 SCH:

O CONHCH3 S Q E 10 References Cited UNITED STATES PATENTS 2,362,508 11/1944 Stevens et a1. 260479 2,701,253 2/1955 Jones et al 260327 2,776,197 1/1957 Gysin et al. 712.4 2,820,799 1/1958 Wagner 2603 2,992,967 7/1961 Haubein 167-30 3,012,933 12/1961 Phillips 167-30 3,062,868 11/1962 Moore et a1 260479 3,066,163 11/1962 Ospenson et al 260479 FOREIGN PATENTS 1,275,658 10/ 1961 France.

912,895 12/ 1962 Great Britain.

OTHER REFERENCES Kolbezen et al., Journal of Agricultural and Food Chemistry, vol. 2, pp. 864-870 (1954).

Metcalf, Pest Control, vol. 30, pp. 20, 26 and 28 (June 1962).

RICHARD K. JACKSON, Primary Examiner.

JULIAN S. LEVITT, LEON ZITVER, LORRAINE A.

WEINBERGER, Examiners.

G. A. MENTIS, I. R. PELLMAN, K. ROSE,

Assistant Examiners.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,349,115 October 24, 1967 Edward D. Weil et a1.

It is hereby certified that error appears in the above numbered p2 ent requiring correction and that the said Letters Patent should read a corrected below.

Column 3, lines 15 to 21, for that portion of the formula reading 7 l S(O) R read 8(0) R line 75, after "above" insert about column 4, line 22, for "trithiocarbanates" read trithiocarbonates column 6,

line 70, the formula should appear as shown below instead of as in the patent:

C H OS C1 column 7, line 21, the formula should appear as shown below instead of as in the patent:

column 8, line 44, for "degree centrigrade" read degrees Centigrade; line 70,"for "groups read group Signed and sealed this 22nd day of July 1969.

(SEAL) Attest:

EDWARD M.FLETCHER,JR. WILLIAM E. SCHUYLER, JR Attesting Officer Commissioner of Patents

Claims

1. NEW COMPOSITIONS OF THE FORMULA: