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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058538생성일: 2026년 10월 26일

Bisphenol A → Sebacic Acid

https://huagongshe.com/reaction/1058538

반응식

참여 물질

역할이름HCID투입량
반응물Bisphenol AHCID 6623—
반응물Dimethyl sebacateHCID 7829—
반응물Trimethyl PhosphateHCID 10541—
반응물Oxo(oxostibanyloxy)stibaneHCID 27652—
반응물Dimethyl-2,6-naphthalenedicarboxylateHCID 61225—
촉매Manganese acetate tetrahydrateHCID 93021—
용매Ethylene GlycolHCID 174—
용매MethanolHCID 887—
생성물Sebacic AcidHCID 5192—
생성물Bisphenol AHCID 6623—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518004B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-832781fb6f304d9ab43d6a66d2f9a938
출처 메모uspto-grants-2003_02