439479
1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
>95% in F+ active
Synonym(s):
N-Chloromethyl-N′-fluorotriethylenediammonium bis(tetrafluoroborate), F-TEDA
About This Item
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form
powder
reaction suitability
reagent type: catalyst
reagent type: oxidant
reaction type: C-H Activation
greener alternative product characteristics
Catalysis
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sustainability
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concentration
>95% in F+ active
mp
260 °C (lit.)
greener alternative category
storage temp.
2-8°C
SMILES string
F[B-](F)(F)F.F[B-](F)(F)F.F[N+]12CC[N+](CCl)(CC1)CC2
InChI
1S/C7H14ClFN2.2BF4/c8-7-10-1-4-11(9,5-2-10)6-3-10;2*2-1(3,4)5/h1-7H2;;/q+2;2*-1
InChI key
TXRPHPUGYLSHCX-UHFFFAOYSA-N
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General description
Application
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.
- As a fluorinating reagent that effects oxidative ring opening of 2,5-diarylfurans to cis-1,4-enediones.
- For direct fluorination of silyl ketene acetals leading to the formation of α-fluoro-α-arylcarboxylic acids.
- As an electrophilic fluorinating reagent used. e.g. in the preparation of fluorinated acylsilanes.
Citation
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
Certificates of Analysis (COA)
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Articles
The importance of selectively fluorinating compounds in medicinal chemistry, biology, and organic synthesis is well appreciated and provides a major impetus to the discovery of new and mild fluorinating agents that can operate safely and efficiently.
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