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HRID 48533생성일: 2026년 10월 23일

Sulfuric Acid → 1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acid

https://huagongshe.com/ko/reaction/48533

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Terephthalic AcidHCID 7489—
반응물1,3,5-TrioxaneHCID 8081—
용매Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
생성물1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acidHCID 7851770.4%

반응 단계

To 153 ml of fuming sulfuric acid, containing about 27% of SO3, 50 g (0.3 m) of terephthalic acid are added, under stirring, at room temperature, then 23 g (0.25 m) of 1,3,5-trioxane are added thereinto in two portions, by cooling to a temperature of 15-18° C. after any addition. At the end of the addition, the mixture is left 30 minutes under stirring at room temperature, then it is heated at 135-145° C. and let under stirring for 2-2.5 hours at this temperature until the end of the reaction. The reaction mixture is cooled to a temperature lower than 3° C., then 100 ml of glacial acetic are added thereto by keeping the temperature at about 25° C. At the end of the addition, the mixture is let to stand 60 minutes under stirring at 20-25° C. and filtered. The wet product is suspended in 1900 ml of water. The suspension is heated up to 25-30° C. under stirring, its pH is adjusted to about 8 by gradual addition of 175 g of sodium bicarbonate. The solid is filtered off on Celite® by washing with hot water (40-45° C.). The pH of the mother liquors is brought to 1.5 by addition of about 125 ml of 37% hydrochloric acid and the obtained precipitate is filtered at 20-25° C. by washing with water until the filtrate reaches a neutral pH. Thus, 32 g of 5-carboxyphthalide with a titer (HPLC)>93% are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703516B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-dc45d70a88db4445bdbe6860ec86d276
출처 메모uspto-grants-2004_03