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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058538Generated: October 26, 2026

Bisphenol A → Sebacic Acid

https://huagongshe.com/reaction/1058538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisphenol AHCID 6623—
ReactantDimethyl sebacateHCID 7829—
ReactantTrimethyl PhosphateHCID 10541—
ReactantOxo(oxostibanyloxy)stibaneHCID 27652—
ReactantDimethyl-2,6-naphthalenedicarboxylateHCID 61225—
CatalystManganese acetate tetrahydrateHCID 93021—
SolventEthylene GlycolHCID 174—
SolventMethanolHCID 887—
ProductSebacic AcidHCID 5192—
ProductBisphenol AHCID 6623—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518004B2
Source datasetuspto-grants-2003_02
ORD IDord-832781fb6f304d9ab43d6a66d2f9a938
Source noteuspto-grants-2003_02