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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2254863생성일: 2026년 10월 26일

Oxygen → Tetrahydrophthalic anhydride

https://huagongshe.com/reaction/2254863

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 gas phase aeration method. Thus, the air in a 300-ml four-necked flask equipped with a stirrer, thermometer, condenser, a dropping funnel for feeding crude trans-1,3-pentadiene, and an unreactive fraction recovery vessel was replaced with nitrogen and, then, the flask was charged with 98 g of maleic anhydride, 500 ppm of p-tert-butylcatechol by way of radical polymerization inhibitor and 1000 ppm of dilauryl thiodipropionate as auxiliary polymerization inhibitor. The charge was melted at 50° to 55° C. and after the internal atmosphere was replaced with nitrogen gas, nitrogen gas containing 4% of oxygen was passed through the gas phase at a rate of 10 ml/min throughout the reaction period. 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 50° to 55° C. over a period of 4 hours. During the reaction, major portion of unreactive fractions was distilled off from the reaction system. After completion of addition, the reaction was conducted at 70° C. for 30 minutes. After completion of the reaction, the reaction mixture was distilled at 85° C. under atmospheric pressure and, then, under reduced pressure to remove the volatile fraction. In this manner, 164 g of 3Me--THPA was obtained. 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-4b050eb4c3be4500bf9d93c525f53888
출처 메모uspto-grants-1993_08