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Tetrabutylammonium fluoride

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Related articles

  • What is Tetrabutylammonium fluoride?
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Tetrabutylammonium fluoride Basic information
Product Name:Tetrabutylammonium fluoride
Synonyms:TETRA-N-BUTYLAMMONIUM FLUORIDE: 75% W/W AQUEOUS SOLUTION;TETRABUTYL AMMONIUM FLUORIDE IN THF (I M);Tetrabutylammonium fluoride;TETRA BUTYL AMMONIUM FLUORIDE (1M SOLUTION IN THF);TBAF;TETRABUTYLAMMONIUM FLUORIDE HYDRATE;Tetra-n-butylammonium fluoride, 75% w/w aq. soln.;Tetrabutylammonium Fluoride (1mol/L in Tetrahydrofuran) [for Catalyst of acylation, silylation and cleavage of Silyl Ether]
CAS:429-41-4
MF:C16H36FN
MW:261.46
EINECS:207-057-2
Product Categories:metal halide;quarternary ammonium salts;Reagents;Silica Gel;Supported Synthesis;Fluoride SourcesSupported Synthesis;Deprotecting Reagents;Others;Protection and Derivatization;Supported Reagents;Fluorinating Reagents;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Nucleophilic Fluorinating Reagents;Ammonium Fluorides (Quaternary);Fluorination;Halogenation;Quaternary Ammonium Compounds;Synthetic Organic Chemistry;bc0001;KT00001
Mol File:429-41-4.mol
Tetrabutylammonium fluoride Structure
Tetrabutylammonium fluoride Chemical Properties
Melting point 62-63 °C(lit.)
density 0.953 g/mL at 25 °C
refractive index n20/D 1.456
Fp 1 °F
storage temp. 2-8°C
solubility Miscible with terahydrofuran, acetonitrile, dimethyl sulfoxide and organic solvents.
form Solution
color Clear light greenish to brown
Water Solubility Insoluble in water.
Sensitive Hygroscopic
Merck 14,9187
BRN 3570522
Exposure limitsACGIH: TWA 2.5 mg/m3
NIOSH: IDLH 250 mg/m3
InChI1S/C16H36N.FH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1
InChIKeyFPGGTKZVZWFYPV-UHFFFAOYSA-M
SMILES[F-].CCCC[N+](CCCC)(CCCC)CCCC
CAS DataBase Reference429-41-4(CAS DataBase Reference)
EPA Substance Registry System1-Butanaminium, N,N,N-tributyl-, fluoride (429-41-4)
Safety Information
Hazard Codes C,F,Xi
Risk Statements 34-19-11-36/37/38-40-37
Safety Statements 26-27-36/37/39-45-33-29-16-36
RIDADR UN 3261 8/PG 2
WGK Germany 3
3
Hazard Note Flammable/Irritant
TSCA TSCA listed
HazardClass 3
PackingGroup II
HS Code 29239000
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Chronic 3
Eye Irrit. 2
Repr. 2
Skin Irrit. 2
MSDS Information
ProviderLanguage
TBAF English
SigmaAldrich English
Tetrabutylammonium fluoride Usage And Synthesis
Chemical PropertiesClear light greenish to amber or brown solution
UsesCatalyst for etherification of alcohols and phenols with alkyl halides Catalyst for benzylation reactions.
UsesTetrabutylammonium fluoride is a reagent in organic syntheses in addition, condensation, base-catalyzed cyclization reactions, fluorination and desulfonylation reactions and as a deprotecting agent. Typically dried prior to use.
UsesTetrabutylammonium fluoride (TBAF) is a commonly used organic soluble fluoride salt. It is used as a base, a phase transfer catalyst, and as a fluoride source. In the research field of fluoride sensor development, TBAF is used as an easy to handle and measurable fluoride anion source. The fluoride in TBAF, once dissolved, can be thought of as a free fluoride with little interaction with the ammonium cation. Since TBAF should not absorb light at wavelengths greater than 240nm, it is useful to monitor sensing reactions with visible spectroscopy.
DefinitionChEBI: Tetrabutylammonium fluoride is a fluoride salt and a tetrabutylammonium salt. It has a role as a phase-transfer catalyst.
Synthesis
hexafluorobenzene

392-56-3

TETRABUTYLAMMONIUM CYANIDE

10442-39-4

Benzenehexacarbonitrile

1217-44-3

Tetrabutylammonium fluoride

429-41-4

Synthesis of TBAF; Anhydrous tetrabutylammonium fluoride (TBAF):; 0.67 g of tetrabutylammonium cyanide (TBACN) was dissolved in 2.5 ml of tetrahydrofuran (THF) and the resulting solution was cooled to -65 °C. In a separate vessel, 0.3 mL of hexafluorobenzene (C6F6) was dissolved in 0.5 mL of THF and cooled to -65°C. The hexafluorobenzene solution was slowly added to the cooled TBACN solution and the mixture was gradually warmed (over 4 hours) to -15°C. During the reaction, the solution changed from colorless to yellow-green and precipitated a white solid. The mixture was cooled again to -65 °C, the solid was collected by filtration and washed twice with cold THF. All separation operations need to be carried out below -36°C. The resulting white or light yellow TBAF solid can be stored in a refrigerator at -36°C for a short period of time. If the reaction mixture is used directly, the overall yield of TBAF exceeds 95% (based on TBACN, as verified by burst experiments with benzyl chloride). Isolated yields of the solid product ranged from 40% to 70%, depending on the efficiency of the washing and filtration steps.1H NMR ((CD3)2SO) δ 3.23 (8H, m), 1.56 (8H, m), 1.28 (8H, sextuple peak, J = 7.31 Hz), 0.86 (12H, t, J = 7.31 Hz); 19F NMR ((CD3)2SO) δ -72.6 ppm(s); 13C NMR ((CD3)2SO) δ 57.5, 23.1, 19.2, 13.5 ppm.

References[1] Patent: US2006/89514, 2006, A1. Location in patent: Page/Page column 5
[2] Patent: US2006/89514, 2006, A1. Location in patent: Page/Page column 5
[3] Patent: US2006/89514, 2006, A1. Location in patent: Page/Page column 5
[4] Patent: US2006/89514, 2006, A1. Location in patent: Page/Page column 5
[5] Patent: US2006/89514, 2006, A1. Location in patent: Page/Page column 5
Tag:Tetrabutylammonium fluoride(429-41-4) Related Product Information
TETRABUTYLAMMONIUM FLUORIDE HYDRATE,TETRABUTYLAMMONIUM FLUORIDE TRIHYDRATE,Tetrabutylammonium fluoride trihydrate 97% TETRABUTYLAMMONIUM FLUORIDE TETRABUTYL AMMONIUM BROMIDE Ammonium hydrogen difluoride Tetrabutylammonium iodide FLUORIDE STANDARD Ammonium fluoride Tetrabutylammonium perchlorate Tetrabutylammonium bromide Tetrabutylammonium hydrogen sulfate Tetrabutylammonium acetate Tetrabutylammonium tetra (tert butyl alcohol) coordination fluoride Tetrabutylammonium hexafluorophosphate Tetrabutylammonium tribromide Tetrabutylammonium nitrate Aluminum fluoride Tetrabutylammonium hydroxide Tetrabutylphosphonium bromide

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