4,4'-이소프로필리덴비스[2-메틸페놀]

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4,4'-이소프로필리덴비스[2-메틸페놀] MSDS

• 2,2-Bis(4-hydroxy-3-methylphenyl)propane

4,4'-이소프로필리덴비스[2-메틸페놀] 화학적 특성, 용도, 생산

• 개요

  2,2-Bis(4-hydroxy-3-methylphenyl)propane is a monomer of polycarbonate and bisphenol A. It has been used as a reaction solution for sodium salt and calcium stearate. The product contains hydrogen chloride and hydrochloric acid as byproducts. This product also reacts with fatty acids to produce aromatic hydrocarbons.

• 화학적 성질

  Powder or crystalline or crystalline powder or chunks

• 용도

  Used as a color-developer in thermosensitive recording materials.

• 제조 방법

  The preparation of 2,2-Bis(4-hydroxy-3-methylphenyl)propane is as follows:In a full-jacket type 1 L separable flask equipped with a thermometer, a stirrer, and a 100 mL dropping funnel, 26.1 g (0.4 mol) of isopropyl alcohol was added under a nitrogen atmosphere, and then 58.3 g (0.5 mol) of 90% by weight sulfuric acid was slowly added thereto. Thereafter, 54.5 g of toluene, 191.5 g (1.8 mol) of ortho-cresol, and 5.5 g (0.03 mol) of dodecanethiol were added thereto, followed by setting the temperature in the separable flask to 40° C. In the dropping funnel, 42.5 g (0.7 mol) of acetone was placed, and it was slowly fed dropwise to the separable flask for 30 minutes. After completion of the dropwise addition of acetone, the reaction was allowed to proceed at 40° C. for 2 hours. After completion of the reaction, 100.0 g of toluene and 100.0 g of demineralized water were fed, and the temperature was increased to 80° C. After the temperature reached 80° C., the reaction liquid was left to stand to confirm that the precipitates generated during the reaction were dissolved into the organic phase and the aqueous phase. This was followed by extraction of the aqueous phase in the lower layer. Thereafter, saturated sodium hydrogen carbonate solution was added to the obtained organic phase to allow neutralization, followed by confirming that the pH of the aqueous phase in the lower layer, became not less than 9. After extraction of the aqueous phase in the lower layer, demineralized water was added to the obtained organic phase, and the resulting mixture was stirred for 10 minutes. Thereafter, the mixture was left to stand, and the aqueous phase was extracted. Part of the obtained organic phase was removed, and subjected to high-performance liquid chromatography to analyze the amount of bisphenol C produced. As a result, the reaction yield in terms of acetone was found to be 84 mol %.

  

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