추천 제품
Quality Level
분석
95%
양식
liquid
density
1.584 g/mL at 25 °C
작용기
fluoro
triflate
저장 온도
2-8°C
SMILES string
O=S(OC(F)F)(C(F)(F)F)=O
InChI
1S/C2HF5O3S/c3-1(4)10-11(8,9)2(5,6)7/h1H
InChI key
DAANAKGWBDWGBQ-UHFFFAOYSA-N
일반 설명
Difluoromethyl triflate (HCF2OTf) is an easy to handle, air-stable and non-ozone-depleting liquid reagent for difluoromethylation. It can be prepared by reacting trifluoromethyltrimethylsilane (TMSCF3) and triflic acid in the presence of titanium tetrachloride (TiCl4).
애플리케이션
Difluoromethyl triflate (TfO-CHF2) can be used as a reagent:
It allows for a simple method toward the preparation of difluoromethyl ethers and thioethers under basic conditions from alcohols and thiols. Difluoromethyl phenols can also be obtained in a single pot from boronic acids and C-H activation of arenes.
- In difluoromethylation reaction.
- To prepare difluoromethoxylated heterocycles by reacting with hydroxylated N-based heterocycles.
- To synthesize trifluoromethylated arenes by treating with diaryliodonium salts in the presence of copper and tetrabutylammonium difluorotriphenylsilicate (TBAT).
It allows for a simple method toward the preparation of difluoromethyl ethers and thioethers under basic conditions from alcohols and thiols. Difluoromethyl phenols can also be obtained in a single pot from boronic acids and C-H activation of arenes.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
135.0 °F
Flash Point (°C)
57.22 °C
이미 열람한 고객
Difluoromethoxylation of N-Heteroaromatics
Snieckus V and Richardson P
Synfacts, 14(03), 0239-0239 (2018)
Difluoromethyl Triflate
Besset T
Encyclopedia of Reagents for Organic Synthesis, Second Edition, 203(03), 1-1 (2001)
Synthesis of difluoromethyl ethers with difluoromethyltriflate.
Patrick S Fier et al.
Angewandte Chemie (International ed. in English), 52(7), 2092-2095 (2013-01-12)
Tri-and difluoromethoxylated N-based heterocycles- Synthesis and insecticidal activity of novel F3CO-and F2HCO-analogues of Imidacloprid and Thiacloprid
Landelle G, et al.
Journal of Fluorine Chemistry, 203(03), 155-165 (2017)
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