933-52-8Relevant articles and documents
Episulfidation of trans-Cyclooctene with an 1,2,4-Oxadithiolane
Adam, Waldemar,Bargon, Rainer M.,Mloston, Grzegorz
, p. 4012 - 4015 (2003)
The dipolar cycloaddition of thiobenzophenone S-oxide (1) and 2,2,4,4-tetramethyl-3-thioxocyclobutanone (2) generates the labile 1,2,4-oxadithiolane I, which in the presence of trans-cyclooctene (3) affords trans-episulfide (9). In this direct sulfur tran
Huisgen,Otto
, p. 5342 (1968)
The fluoride anion-catalyzed sulfurization of thioketones with elemental sulfur leading to sulfur-rich heterocycles: First sulfurization of thiochalcones ?
Bielinski, Dariusz M.,Heimgartner, Heinz,Mloston, Grzegorz,Urbaniak, Katarzyna,Wreczycki, Jakub
, (2021/06/12)
Fluoride anion was demonstrated as a superior activator of elemental sulfur (S8) to perform sulfurization of thioketones leading to diverse sulfur-rich heterocycles. Due to solubility problems, reactions must be carried out either in THF using tetrabutylammonium fluoride (TBAF) or in DMF using cesium fluoride (CsF), respectively. The reactive sulfurizing reagents are in situ generated, nucleophilic fluoropolysulfide anions FS(8?x)?, which react with the C=S bond according to the carbophilic addition mode. Dithiiranes formed thereby, existing in an equilibrium with the ring-opened form (diradicals/zwitterions) are key-intermediates, which undergo either a step-wise dimerization to afford 1,2,4,5-tetrathianes or an intramolecular insertion, leading in the case of thioxo derivatives of 2,2,4,4-tetramethylcyclobutane-1,3-dione to ring enlarged products. In reactions catalyzed by TBAF, water bounded to fluoride anion via H-bridges and forming thereby its stable hydrates is involved in secondary reactions leading, e.g., in the case of 2,2,4,4-tetramethyl-3-thioxocyclobutanone to the formation of some unexpected products such as the ring enlarged dithiolactone and ring-opened dithiocarboxylate. In contrast to thioketones, the fluoride anion catalyzed sulfurization of their α,β-unsaturated analogues, i.e., thiochalcones is slow and inefficient. However, an alternative protocol with triphenylphosphine (PPh3) applied as a catalyst, offers an attractive approach to the synthesis of 3H-1,2-dithioles via 1,5-dipolar electrocyclization of the in situ-generated α,β-unsaturated thiocabonyl S-sulfides. All reactions occur under mild conditions and can be considered as attractive methods for the preparation of sulfur rich heterocycles with diverse ring-size.
Tetramethylcyclobutanedione and tetramethylcyclobutane diol Method for manufacturing the same
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Paragraph 0043-0074, (2021/09/29)
The invention provides tetramethylcyclobutanedione and tetramethylcyclobutane diol, and a manufacturing method thereof. The present invention provides the following method. 2, 2, 4, 4 - Tetramethylcyclobutane -1, 3 - diketones can be easily produced by carrying out the dimerization reaction of the dimethylketene in a solvent suitable for the actual production (reaction time) by easily treating and general low boiling solvent in the production process. The dimerization reaction of the dimethyl ketene can be accelerated, and the time required for solvent removal can be shortened as compared with the high-boiling solvent. Compared with the prior art, the manufacturing can be performed in a short time.
PROCESS FOR PREPARING 2,2,4,4-TETRAMETHYL-1,3-CYCLOBUTANEDIOL
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Paragraph 0119-0159, (2019/10/08)
Disclosed is a method for preparing 2,2,4,4-tetramethyl-1,3-cyclobutanediol, which prepares (E) 2,2,4,4-tetramethyl-1,3-cyclobutanediol (CBDO) which is a final material by sequentially going through (A) methacrylic acid (MAA) as a raw material, and (B) isobutyric acid (IBA), (C) isobutyric anhydride (IBAN), and (D) 2,2,4,4-tetramethyl-1,3-cyclobutanedione (CBDK) as an intermediate. According to the present invention, the method for preparing 2,2,4,4-tetramethyl-1,3-cyclobutanediol which is economical and eco-friendly by optimizing preparation steps and maximizing the efficiency is provided.COPYRIGHT KIPO 2019