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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2254864생성일: 2026년 10월 26일

Oxygen → Tetrahydrophthalic anhydride

https://huagongshe.com/reaction/2254864

반응식

참여 물질

역할이름HCID투입량
반응물OxygenHCID 977—
반응물4-tert-ButylcatecholHCID 7381—
반응물Maleic AnhydrideHCID 7923—
반응물Propanoic acid, 3,3'-thiobis-, didodecyl esterHCID 31250—
반응물1,3-PentadieneHCID 62204—
생성물Tetrahydrophthalic anhydrideHCID 6810—

반응 단계

3Me--THPA was produced by the liquid phase aeration method. Thus, the air in a 300 ml four-necked flask similar to the one used in Example 5 was replaced with nitrogen and, then, the flask was charged with 98 g of maleic anhydride, 300 ppm of p-tert-butylcatechol by way of auxiliary polymerization inhibitor and 800 ppm of dilauryl thiodipropionate by way of auxiliary polymerization inhibitor and the charge was melted at 60° C. Then, the internal atmosphere of the reaction system was replaced with nitrogen gas, and thereafter nitrogen gas containing 1 volume % of oxygen was passed into the reaction mixture at a rate of 5 ml/min throughout the reaction. Under this atmosphere, 374 g of crude trans-1,3-pentadiene of the same composition as that used in Example 1 was continuously added at 60° C. for 4 hours. Major portion of unreactive fractions was distilled off from the reaction mixture in the course of reaction. Thereafter, the reaction mixture was treated in the same manner as in Example 5 to give 164 g of 3Me--THPA. The investigation revealed no gels in the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05237074
출처 데이터셋uspto-grants-1993_08
ORD IDord-a2b09e0aab0147408fda825908cb4e7e
출처 메모uspto-grants-1993_08