GB1114104A - 1,2,3-trihydro-2-bora-1,3,5-triazines and process for their manufacture - Google Patents
1,2,3-trihydro-2-bora-1,3,5-triazines and process for their manufactureInfo
- Publication number
- GB1114104A GB1114104A GB5455466A GB5455466A GB1114104A GB 1114104 A GB1114104 A GB 1114104A GB 5455466 A GB5455466 A GB 5455466A GB 5455466 A GB5455466 A GB 5455466A GB 1114104 A GB1114104 A GB 1114104A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- alkyl
- phenyl
- contain
- substituted
- 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
- XBZBMCJOGOVFSI-UHFFFAOYSA-N N1BNCN=C1 Chemical class N1BNCN=C1 XBZBMCJOGOVFSI-UHFFFAOYSA-N 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000000843 powder Substances 0.000 abstract 3
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000012141 concentrate Substances 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000000080 wetting agent Substances 0.000 abstract 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 150000001639 boron compounds Chemical class 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 abstract 1
- 238000010410 dusting Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- -1 ethoxylated alkyl phenol Chemical compound 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 239000003495 polar organic solvent Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
The invention comprises 1,2,3-trihydro-2-bora-1,3,5-triazines of the general formula <FORM:1114104/C2/1> in which R1 and R2 represent hydrogen, alkyl, individually or together a cycloalkyl radical which contain up to 8 carbon atoms and may include oxygen as a hetero atom or a phenyl radical which may be substituted, and R3 is a phenyl group or, if at least one of the substituents R1 and R2 is other than hydrogen, an alkyl radical with up to 8 carbon atoms. These compounds and others having the general Formula I, in which R1 and R2 represent hydrogen, alkyl, together or separately a cycloalkyl, radical which may contain a hetero atom, or a phenyl radical which may be substituted, and R3 represents hydrogen, a C1-C8 alkyl radical or phenyl, are prepared by heating a guanidine of formula <FORM:1114104/C2/2> with a boron compound of formula B(OR3)3. The products obtained may be subjected to an ester interchange reaction with other alcohols.ALSO:Herbicidal compositions comprise, as active ingredient, at least one 1,2,3-trihydro-2-bora-1,3,5-triazine of the general formula <FORM:1114104/A5-A6/1> in which R1 and R2 represent hydrogen, alkyl and individually or jointly a cycloalkyl radical which may contain a hetero atom, or phenyl radicals which may be substituted, and R3 represents hydrogen, a C1-C8 alkyl radical or a phenyl radical. The compositions may be applied in the form of emulsion concentrates, wettable powders or dusting powders. The emulsion concentrates contain an anhydrous strongly polar organic solvent, e.g. tetrahydrofuran, formamide or dimethyl formamide, either alone or with a wetting agent, for example ethoxylated alkyl phenol. When used as powders the compositions contain conventional inert carriers with, if desired, wetting agents or adhesives.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5455466A GB1114104A (en) | 1966-12-06 | 1966-12-06 | 1,2,3-trihydro-2-bora-1,3,5-triazines and process for their manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5455466A GB1114104A (en) | 1966-12-06 | 1966-12-06 | 1,2,3-trihydro-2-bora-1,3,5-triazines and process for their manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1114104A true GB1114104A (en) | 1968-05-15 |
Family
ID=10471394
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5455466A Expired GB1114104A (en) | 1966-12-06 | 1966-12-06 | 1,2,3-trihydro-2-bora-1,3,5-triazines and process for their manufacture |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1114104A (en) |
-
1966
- 1966-12-06 GB GB5455466A patent/GB1114104A/en not_active Expired
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