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439479

Sigma-Aldrich

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)

greener alternative

>95% in F+ active

Synonym(s):

N-Chloromethyl-N′-fluorotriethylenediammonium bis(tetrafluoroborate), F-TEDA

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0.25 ML
CN¥4,591.71
1.7 ML
CN¥15,409.58

CN¥4,591.71

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0.25 ML
CN¥4,591.71
1.7 ML
CN¥15,409.58

About This Item

Empirical Formula (Hill Notation):
C7H14B2ClF9N2
CAS Number:
140681-55-6
Molecular Weight:
354.26
Beilstein:
5368649
MDL number:
MFCD00142607
UNSPSC Code:
12352101
PubChem Substance ID:
24867509
NACRES:
NA.22

CN¥4,591.71

Please contact Customer Service for Availability
Request a Bulk Order

form

powder

reaction suitability

reagent type: catalyst
reagent type: oxidant
reaction type: C-H Activation

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

concentration

>95% in F+ active

mp

260 °C (lit.)

functional group

chloro

greener alternative category

Aligned,

storage temp.

2-8°C

SMILES string

F[B-](F)(F)F.F[B-](F)(F)F.F[N+]12CC[N+](CCl)(CC1)CC2

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is a fluorine donor also called Selectfluor and has been enhanced for catalysis. Find details here.

Application

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) is an electrophilic fluorinating reagent used for greener fluorination of acetoacetamides in PEG-400.
Catalyst-free and highly selective electrophilic mono-fluorination of acetoacetamides: facile and efficient preparation of 2-fluoroacetoacetamides in PEG-400

It can be used:
  • As a highly effective and versatile source of electrophilic fluorine.[1]
  • As a fluorinating reagent that effects oxidative ring opening of 2,5-diarylfurans to cis-1,4-enediones.[2]
  • For direct fluorination of silyl ketene acetals leading to the formation of α-fluoro-α-arylcarboxylic acids.[3]
  • As an electrophilic fluorinating reagent used. e.g. in the preparation of fluorinated acylsilanes.[4]

Other Notes

First application of ionic liquids in electrophilic fluorination of arenes; Selectfluor (F-TEDA-BF4) for “green” fluorination.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H317,H318,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    WXBF2512V
    WXBF0589V
    WXBD7959V
    MKCR9380
    MKCR5622

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    A novel general method for preparation of a-fluoro-a-arylcarboxylic acid. Direct fluorination of silyl ketene acetals with Selectfluor
    Zhang F and Song JZ
    Tetrahedron Letters, 47(43), 7641-7644 (2006)
    Rajendra P Singh et al.
    Accounts of chemical research, 37(1), 31-44 (2004-01-21)
    Synthetic and structural aspects of organofluorine compounds continue to be the focal points of vigorous research activities, as evidenced by the appearance of a large number of publications. Among the various useful methodologies for the introduction of fluorine into organic
    Oxidative ring opening of 2, 5-diarylfurans by Selectfluor
    Blank SJ and Stephens CE
    Tetrahedron Letters, 47(38), 6849-6850 (2006)
    Paul T Nyffeler et al.
    Angewandte Chemie (International ed. in English), 44(2), 192-212 (2004-12-04)
    The replacement of hydrogen atoms with fluorine substituents in organic substrates is of great interest in synthetic chemistry because of the strong electronegativity of fluorine and relatively small steric footprint of fluorine atoms. Many sources of nucleophilic fluorine are available
    A general method for synthesis of trifluoroacetyltrialkyl (aryl) silanes and the Sakurai reaction of fluorinated acylsilanes with allyl silanes
    Chung WJ and Welch JT
    Journal of Fluorine Chemistry, 125(4), 543-548 (2004)
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