- Preparation method of phospholene oxide, substituted phospholene oxide and preparation method of substituted phospholene oxide
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The invention relates to a preparation method of phospholene oxide, substituted phospholene oxide and a preparation method of the substituted phospholene oxide and belongs to the technical field of organic synthesis. The preparation method of the phospholene oxide comprises the following steps: 1) enabling phosphorus trihalide and chloroethanol to react at -10 to 40 DEG C for 0.5 to 3h so as to obtain a compound shown as a formula I; 2) enabling the compound shown as the formula I, a catalyst, a polymerization inhibitor and 1,3-butadiene to react at room temperature for 4 to 10h; then raisingthe temperature to 40 to 80 DEG C and reacting for 12 to 24h; then raising the temperature to 80 to 100 DEG C and reacting for 8 to 14h to obtain the phospholene oxide. The e preparation method of thephospholene oxide, provided by the invention, takes the phosphorus halide and the chloroethanol as raw materials, and the raw materials are easy to obtain and the price is low; reaction conditions are moderate and the method is simple and feasible and is low-cost.
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Paragraph 0056-0058; 0062-0063; 0064-0071; 0072-0079
(2019/11/12)
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- 1,4,2-Diazaphospholidine-3,5-diones and related compounds: A lecture on unpredictability in catalysis
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1,4,2-diazaphospholidine-3,5-diones and related compounds and unpredictability in catalysis was studied. The five-membered ring species 4 6, which are all readily accessible by the McCormack reaction, optionally with subsequent hydrogenation, were selected for this study. The use of saturated species of type 4 (1-organyl-phospholanes) as catalysts led to a complete reverse in the selectivity of the reaction, in favor of the formation of the isocyanate trimers. Owing to the high activity of the corresponding P-oxides in carbodiimidization reactions, it can be assumed that the findings can be attributed to partial air oxidation of the trivalent phosphorus species applied. The symmetrical species 6, in total contrast to the other two members of the series, do not exhibit any catalytic activity with respect to isocyanates and instead react cleanly with two equivalents of isocyanate to effect the extrusion of 1,3-diene.
- Richter, Frank U.
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supporting information; experimental part
p. 5200 - 5202
(2009/12/24)
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