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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1058538Erstellt: 25. Oktober 2026

Bisphenol A → Sebacic Acid

https://huagongshe.com/reaction/1058538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBisphenol AHCID 6623—
EduktDimethyl sebacateHCID 7829—
EduktTrimethyl PhosphateHCID 10541—
EduktOxo(oxostibanyloxy)stibaneHCID 27652—
EduktDimethyl-2,6-naphthalenedicarboxylateHCID 61225—
KatalysatorManganese acetate tetrahydrateHCID 93021—
LösungsmittelEthylene GlycolHCID 174—
LösungsmittelMethanolHCID 887—
ProduktSebacic AcidHCID 5192—
ProduktBisphenol AHCID 6623—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06518004B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-832781fb6f304d9ab43d6a66d2f9a938
Quellennotizuspto-grants-2003_02