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HRID 1058538作成日:2026年10月27日

Bisphenol A → Sebacic Acid

https://huagongshe.com/reaction/1058538

反応式

関与物質

役割名称HCID仕込み量
反応物Bisphenol AHCID 6623—
反応物Dimethyl sebacateHCID 7829—
反応物Trimethyl PhosphateHCID 10541—
反応物Oxo(oxostibanyloxy)stibaneHCID 27652—
反応物Dimethyl-2,6-naphthalenedicarboxylateHCID 61225—
触媒Manganese acetate tetrahydrateHCID 93021—
溶媒Ethylene GlycolHCID 174—
溶媒MethanolHCID 887—
生成物Sebacic AcidHCID 5192—
生成物Bisphenol AHCID 6623—

反応手順

Dimethyl 2,6-naphthalenedicarboxylate and dimethyl sebacate were dispersed in ethylene glycol and an addition product of two ethylene oxides tobisphenol A (BPA•2EO). Then, 0.029 part of manganese acetate tetrahydrate, 0.028 parts of antimony trioxide and 0.1% of spherical silica particles having a mean particle size of 0.3 μm were added to 100 parts of the total of dimethyl 2,6-naphthalenedicarboxylate and dimethyl sebacate, and heated with stirring to conduct the reaction. The temperature was elevated to 235° C. while removing methanol produced as a by-product. After the by-production of methanol was completed, 0.03 part of trimethyl phosphate was added thereto. Then, the pressure was reduced to 0.3 Torr while elevating the temperature to 285° C. to conduct the polymerization by changing the reaction time. Dyes described in JP-A-7-168309, compounds I-6 and I-24, were each further added to the solid matter in an amount of 54 ppm. The copolymerization composition ratios of sebacic acid (SA) and BPA•2EO and the intrinsic viscosities of polyesters thus obtained are shown in Table II-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06518004B2
出典データセットuspto-grants-2003_02
ORD IDord-832781fb6f304d9ab43d6a66d2f9a938
出典メモuspto-grants-2003_02