Conditions | Yield |
---|---|
With boric acid In 5,5-dimethyl-1,3-cyclohexadiene Reflux; Inert atmosphere; | 89% |
With boric acid | |
With boric acid; toluene |
Trimethyl borate
triethanolamine
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
In toluene for 1h; Reflux; Inert atmosphere; Large scale; | 87.7% |
triethyl borate
triethanolamine
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
In toluene for 1h; Reflux; | 85.9% |
triethanolamine
Triisopropyl borate
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
In toluene for 1h; Reflux; | 82.9% |
triethanolamine
boric acid
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
In water at 120℃; | 70% |
In benzene azeotropic distn. (reflux); crystn., elem. anal.; | |
In toluene azeotropic distn. (reflux); crystn., elem. anal.; | |
In xylene byproducts: H2O; refluxing with sepn. of H2O; hot filtration, crystn., recrystn. (acetone); | |
In water at 120℃; |
triethanolamine
water
metaboric acid
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
at 10 - 30℃; Equilibrium constant; |
triethoxyphenylsilane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-phenyl-2,8,9-trioxa-5-aza-1-silabicyclo{3.3.3}undecane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 80℃; for 2h; | 95% |
2-Bromoethyl methyl ether
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Tris(3,6-dioxaheptyl)amine
Conditions | Yield |
---|---|
With tetrabutyl-ammonium chloride; sodium hydroxide In sulfolane at 60 - 120℃; Reagent/catalyst; | 92.7% |
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
With aluminum (III) chloride; Triethoxysilane for 4h; Inert atmosphere; Reflux; | 88% |
2-chloroethyl methyl ether
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
Tris(3,6-dioxaheptyl)amine
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; potassium hydroxide In dimethyl sulfoxide at 60 - 120℃; Catalytic behavior; Reagent/catalyst; Solvent; Inert atmosphere; Autoclave; Large scale; | 86.3% |
tetraethoxy orthosilicate
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-ethoxysilatrane
Conditions | Yield |
---|---|
With aluminum isopropoxide In xylene at 140℃; for 3h; | 80% |
2-furyltriethoxysilane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-furan-2-yl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 140℃; for 8h; | 71% |
Triethoxyvinylsilane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-vinylsilatrane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 140℃; for 20h; | 68% |
triethoxy(thiophen-2-yl)silane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
2-silatranylthiophene
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 140℃; for 28h; | 66% |
tri-furan-2-yl-phenyl-silane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-phenyl-2,8,9-trioxa-5-aza-1-silabicyclo{3.3.3}undecane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 80℃; for 3h; | 65% |
hexa-N-methyl-Si-phenyl-silanetriamine
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-phenyl-2,8,9-trioxa-5-aza-1-silabicyclo{3.3.3}undecane
Conditions | Yield |
---|---|
With aluminum isopropoxide In xylene at 140℃; for 10h; | 60% |
5-Methoxy-1-tetralone
ethyl iodide
chromium(0) hexacarbonyl
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
lithium diisopropyl amide
Conditions | Yield |
---|---|
In not given sequential treatment of 5-methoxy-1-tetralone with Cr(CO)6, LiN(i-Pr)2,B(OC2H4)3N, EtI and LiAlH4; further educt: LiAlH4; | 51% |
Methyltriethoxysilan
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-methylsilatrane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 140℃; for 22h; | 50% |
Conditions | Yield |
---|---|
With aluminum (III) chloride; Triethoxysilane In 5,5-dimethyl-1,3-cyclohexadiene Inert atmosphere; | 24% |
With aluminum (III) chloride; Triethoxysilane In 5,5-dimethyl-1,3-cyclohexadiene for 4h; Reflux; | 10.80 g |
Conditions | Yield |
---|---|
Stage #1: sodium; chlorobenzene In hexane at 30℃; for 0.5h; Stage #2: 2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane In tetrahydrofuran; hexane at 0℃; for 0.166667h; | 14% |
Conditions | Yield |
---|---|
Stage #1: (4-Nitrophenyl)acetylene With trimethoxysilane; dihydrogen hexachloroplatinate In isopropyl alcohol; toluene hydrosilylation; Heating; Stage #2: 2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane With aluminium trichloride In xylene for 24h; Esterification; transesterification; Heating; | A 9% B 13% |
chloromethyltriethoxysilane
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
1-(chloromethyl)silatrane
Conditions | Yield |
---|---|
With sodium ethanolate In N,N-dimethyl-formamide at 140℃; for 75h; | 10% |
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
A
perfluorodiethyl ether
B
Perfluoro-N,N-dimethylaminoacetyl fluoride
C
2,2,3,3,5,5,6,6-Octafluoro-4-trifluoromethyl-morpholine
D
2,2-difluoro-2-(2,2,3,3,5,5,6,6-octafluoromorpholin-4-yl)acetyl fluoride
Conditions | Yield |
---|---|
With hydrogen fluoride at 7 - 8℃; for 10.3h; Fluorination; Cyclization; Electrochemical reaction; Further byproducts given; | A 7.5% B 5% C 8.8% D 3.9% |
water
2,8,9-trioxa-5-aza-1-borabicyclo[3.3.3]undecane
A
metaboric acid
Conditions | Yield |
---|---|
at 10 - 30℃; Equilibrium constant; |
The molecular formula of TRIETHANOLAMINE BORATE(283-56-7) is C6H18BN3O3.
Its molecular weight is about 156.9754.And the density of it is 1.13 g/cm3.Melting point is about 235-237 °C,boiling point is about 149.6 °C at 760 mmHg and flash point is about 44.3 °C.The appearance of TRIETHANOLAMINE BORATE(283-56-7) is white .It is the odorless solid and appears white.
The following picture is the structure of TRIETHANOLAMINE BORATE(283-56-7).
1. | ivn-mus LD:>100 mg/kg | EJMCA5 European Journal of Medicinal Chemistry. Chimie Therapeutique. 13 (1978),207. |
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