GB769222A - Esters of dithiocarbamic acids - Google Patents
Esters of dithiocarbamic acidsInfo
- Publication number
- GB769222A GB769222A GB2673854A GB2673854A GB769222A GB 769222 A GB769222 A GB 769222A GB 2673854 A GB2673854 A GB 2673854A GB 2673854 A GB2673854 A GB 2673854A GB 769222 A GB769222 A GB 769222A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloroallyl
- alkyl
- esters
- dithiocarbamic
- group
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/21—Radicals derived from sulfur analogues of carbonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention comprises compositions of esters of dithiocarbamic acid, the amino group being unsubstituted or substituted by one or two alkyl, cycloalkyl, alkenyl, hydroxyalkyl or cyanoalkyl groups of not more than 8 carbon atoms, or bisdithiocarbamic esters with substituents forming a morpholinyl, piperidyl, or pyrrolidyl ring, or (in bis-compounds) a piperazine ring which may be alkylated on the 2- and 5-carbon atoms, the ester group in all cases being a haloalkenyl or haloalkadienyl group; and the dithiocarbamic esters of formula <FORM:0769222/IV(b)/1> in which R1 is hydrogen or one of the groups specified above, R2 is alkyl of 3 to 8 C and R3 is haloalkenyl or haloalkadienyl. The method of preparing the esters is by the reaction between a dithiocarbamic salt corresponding to the above formul and a dihaloalkene or dihaloalkadiene, only one halogen being removed. In examples the 3-chloro-2-butenyl-, 2-chloroallyl-, and 3-chloroallyl - N:N - dimethyldithiocarbamate, 3 - chloro - 2 - butenyldithiocarbamate; 2-chloroallyl-, 3 - chloro - 2 - butenyl -, and 3-chloroallyl - N:N - diethyldithiocarbamate, 3 - chloro - 2 - butenyl - 4 - morpholinecarbodithioate, and similar 2-chloroallyl- and 3-chloroallyl-derivatives, several chloroalkenyl-N:N-diallyl dithiocarbamates, bis-(21-chloroallyl)-2:5 - dimethyl - 1:4 - piperazine - carbodithioate and a table of similar compounds, are prepared by the action of the alkenyl dichlorides on the corresponding sodium or ammonium dithiocarbamic derivatives. Compounds in which the carbamic N is substituted by OH-alkyl and CN-alkyl are included. The products may be employed for weed-killers as sprays, emulsions, and dry compositions, and applied solid to earth and water (see Group VI).ALSO:Herbicidal compositions contain dithiocarbamic esters of the formul <FORM:0769222/VI/1> and <FORM:0769222/VI/2> in which R1 and R2 are hydrogen, alkyl cycloalkyl, alkenyl, hydroxy alkyl or cyanoalkyl, or R1, R2 and the N form a morpholinyl, piperidyl or pyrollidyl group, R3 is haloalkenyl or haloalkadienyl, R4 is hydrogen or alkyl, (see Group IV(b)), and dispersing agents or carriers. Carriers referred to include talc, clay, pyrophyllite and silica, and as solvents for dispersions acetone, chloroform, alcohol, benzene and heptane and other organic liquids. A number of dispersing agents are mentioned.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2673854A GB769222A (en) | 1954-09-15 | 1954-09-15 | Esters of dithiocarbamic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2673854A GB769222A (en) | 1954-09-15 | 1954-09-15 | Esters of dithiocarbamic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB769222A true GB769222A (en) | 1957-03-06 |
Family
ID=10248457
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2673854A Expired GB769222A (en) | 1954-09-15 | 1954-09-15 | Esters of dithiocarbamic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB769222A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3284287A (en) * | 1964-01-29 | 1966-11-08 | Monsanto Co | Inhibiting growth of fungi and bacteria |
-
1954
- 1954-09-15 GB GB2673854A patent/GB769222A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3284287A (en) * | 1964-01-29 | 1966-11-08 | Monsanto Co | Inhibiting growth of fungi and bacteria |
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