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Merck
CN

132063

三乙基胺 三氢氟酸盐

99%

别名:

N,N-Diethylethanamine

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EC Number:
204-469-4
UNSPSC Code:
12352200
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Quality Level

assay

99%

form

liquid

solubility

water: soluble 112 g/L at 20 °C

General description

Triethylamine trihydrofluoride is a non-corrosive reagent. It is a promising source of fluorine and is widely employed in various benzylic fluorination reactions.

Application

Triethylamine trihydrofluoride (TREAT-HF) may be employed as a fluorinating reagent for the following studies:
  • Microwave-assisted transformation of dichloromethyl- and trichloromethyl substrates to the corresponding fluoro analogs.
  • Preparation of 9-(2,3-dideoxy-2-fluoro-β-D-threo-pentofuranosyl)adenine.
  • Synthesis of various fluorinated compounds.
  • Preparation of fluoroamines.


signalword

Danger

target_organs

Respiratory system

存储类别

3 - Flammable liquids

flash_point_f

12.2 °F - closed cup

flash_point_c

-11 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

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Wei Liu et al.
Angewandte Chemie (International ed. in English), 52(23), 6024-6027 (2013-04-26)
An efficient protocol for the selective fluorination of benzylic C-H bonds is described. The process is catalyzed by manganese salen complexes and uses nucleophilic fluorine sources, such as triethylamine trihydrofluoride and KF. Reaction rates are sufficiently high (30 min) to
Asymmetric Synthesis of Fluoroamines from Chiral Aziridines.
Park H, et al.
Bull. Korean Chem. Soc., 35, 699-700 (2014)
Improved synthesis of 9-(2, 3-dideoxy-2-fluoro-β-D-threo-pentofuranosyl) adenine (FddA) using triethylamine trihydrofluoride.
Takamatsu S, et al.
Tetrahedron Letters, 42(12), 2321-2324 (2001)