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HRID 2254863作成日:2026年10月27日

Oxygen → Tetrahydrophthalic anhydride

https://huagongshe.com/reaction/2254863

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物4-tert-ButylcatecholHCID 7381—
反応物Maleic AnhydrideHCID 7923—
反応物Propanoic acid, 3,3'-thiobis-, didodecyl esterHCID 31250—
反応物1,3-PentadieneHCID 62204—
生成物Tetrahydrophthalic anhydrideHCID 6810—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05237074
出典データセットuspto-grants-1993_08
ORD IDord-4b050eb4c3be4500bf9d93c525f53888
出典メモuspto-grants-1993_08