FIELD: chemistry.
SUBSTANCE: invention relates to a method of producing 1,2-diarylethane-1,2-diones of general formula 1:
Ar=Ph (a), m-tolyl – (b), 1-naphthyl – (c), from aromatic acid esters, in the presence of a catalyst, magnesium powder, in tetrahydrofuran, in an argon atmosphere, at atmospheric pressure, according to the invention, the catalyst used is Cp2ZrCl2, the aromatic acid esters used are ArCOOR, where Ar = Ph, R = n-Bu, Ar = m-tolyl, R = Me, Ar = 1-naphthyl, R = Et, reaction is carried out in presence of trimethylchlorosilane (Me3SiCl), with molar ratio ArCOOR:Mg:Zr:Me3SiCl = 1:(1-4):(0.08-0.12):(3-8), at 50 °C, for 6 h.
EFFECT: novel method of producing 1,2-diarylethane-1,2-diones (1) from esters of aromatic acids in presence of magnesium, a catalyst and trimethylchlorosilane, which reduces fire hazard associated with use of EtAlCl2, and obtain 1,2-diarylethane-1,2-diones (1) with output of 81-87%.
1 cl, 1 tbl, 16 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD FOR PRODUCING BENZYL | 2015 |
|
RU2624673C2 |
METHOD FOR OBTAINING N,N-DIMETHYL-4-BIPHENYLAMINE AND ITS DERIVATIVES | 2022 |
|
RU2794095C1 |
METHOD FOR OBTAINING 1-PHENYL-1-BORASPYROALKANE | 2022 |
|
RU2800048C1 |
METHOD OF PREPARING CATALYST FOR OBTAINING 3-ACETYLHEPTANE-2,6-DIONE AND METHOD OF OBTAINING 3-ACETYLHEPTANE-2,6-DIONE WITH APPLICATION OF OBTAINED CATALYST | 2012 |
|
RU2494810C1 |
METHOD OF PRODUCING 3-ALKYL-3-METHYL-1-PHENYL-3-OLS | 2014 |
|
RU2596878C2 |
DISPIROINDOLINONES BASED ON RHODANINES AS P53-MDM2 INHIBITORS OF PROTEIN-PROTEIN INTERACTION | 2019 |
|
RU2730286C1 |
METHOD OF PRODUCING 1,2-DIALKYLBORINANES | 2017 |
|
RU2688195C2 |
METHOD OF PRODUCING 2,3-DIALKYL-1,4-DICYCLOPROPYL-1,4-BUTANEDIONES | 2014 |
|
RU2565789C1 |
METHOD OF PRODUCING DIHALOGEN DERIVATIVE OF 1,2,3,4-TETRAHYDROPYRIDO- OR PYRIDO[1,2-]BENZIMIDAZOLE-6,9-DIONE | 2023 |
|
RU2828349C1 |
METHOD OF PRODUCING α-[(PENTANE-2,4-DION-3-YL)METHOXY]-ω-[(PENTANE-2,4-DION-3-YL)METHYLSULPHANYL] ALKANES | 2014 |
|
RU2605450C2 |
Authors
Dates
2025-06-06—Published
2024-12-24—Filed