C₁₄H₁₄F₃NO₆

Base Information

Chemical Name:C₁₄H₁₄F₃NO₆
CAS No.:1448300-69-3
Molecular Formula:C₁₄H₁₄F₃NO₆
Molecular Weight:349.263
Hs Code.:

C<sub>14</sub>H<sub>14</sub>F<sub>3</sub>NO<sub>6</sub>

Synonyms:C₁₄H₁₄F₃NO₆

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₁₄H₁₄F₃NO₆

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Technology Process of C₁₄H₁₄F₃NO₆

There total 3 articles about C₁₄H₁₄F₃NO₆ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

: 53960-62-6
2-trifluoromethyl-β-nitrostyrene

: 108-59-8
malonic acid dimethyl ester

: 1448300-69-3
C₁₄H₁₄F₃NO₆

Guidance literature:: With Cl^(1-)*C₃₂H₁₂BF₂₄^(1-)*C₆H₅N₂O₂^(1-)*C₄₂H₄₈CoN₆⁽³⁺⁾; In [⁽²⁾H₆]acetone; at 0 ℃; for 24h;
DOI:10.1021/acscatal.1c01883

Reference yield:

: 99696-01-2,93628-97-8
p-trifluoromethyl-trans-β-nitrostyrene

: 108-59-8
malonic acid dimethyl ester

: 916830-75-6
dimethyl 2-(2-nitro-1-(2-trifluoromethylphenyl)ethyl)malonate

: 1448300-69-3
C₁₄H₁₄F₃NO₆

Guidance literature:: With pyridine; Λ-[Co((S,S)-1,2-diphenylethylenediamine)₃]³⁺2Cl^?B(3,5-C₆H₃(CF₃)₂)₄·2H₂O; In neat (no solvent); at 20 ℃; for 0.5h; Overall yield = 99 percent; enantioselective reaction; Milling; Green chemistry;
DOI:10.1039/d1nj03698j

Reference yield:

: 75-52-5
nitromethane

: 447-61-0
2-Trifluoromethylbenzaldehyde

: 108-59-8
malonic acid dimethyl ester

: 916830-75-6
dimethyl 2-(2-nitro-1-(2-trifluoromethylphenyl)ethyl)malonate

: 1448300-69-3
C₁₄H₁₄F₃NO₆

Guidance literature:: With cinchona alkaloid and aminopropyl group-based hybrid organic-inorganic catalyst; In 1,4-dioxane; at 70 ℃; for 36h; Overall yield = 70 %; enantioselective reaction;
DOI:10.1039/c3sc22310h