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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48534Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/48534

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTerephthalic AcidHCID 7489—
Edukt1,3,5-TrioxaneHCID 8081—
EduktSodium BicarbonateHCID 516892—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acidHCID 7851789%

Reaktionsbedingungen

Temperatur131.5 °C

Reaktionsschritte

To 892 g of fuming sulfuric acid, containing 25-27% of SO3, 100 g (0.6 m) of terephthalic acid are added at 20-23° C., under stirring, then 46 g (0.5 m) of 1,3,5-trioxane are added portionwise thereto at about 15° C. At the end of the addition, the mixture is heated 2 hours at 130-133° C. whereby a dark, clear solution is obtained. When the reaction is complete, as shown by a HPLC control, the mixture is cooled to 20-22° C. and 210 g of glacial acetic acid are slowly added thereto, without exceeding the temperature of 23-25° C. The mass is cooled to −5-0° C. and 1800 ml of cold deionized water are added thereto. During this operation the temperature rises to 43-45° C. At the end of the addition, the mixture is kept 1 hour under stirring at 23-25° C., then it is filtered, the solid is washed with deionized water abundantly and suspended, still wet, in 1200 ml of deionized water at room temperature. To the suspension thus obtained, about 1550 g of a 7% solution of NaHCO3 are added to a constant pH of 7,6-7,8. The mixture is filtered on Celite®, washing with deionized water. The pH of the filtrate is brought to about 1 by slow addition of about 120 ml of 35% hydrochloric acid at 22-25° C. The suspension is kept 1 hour under stirring at 22-25° C., then it is filtered and washed with deionized water abundantly. The product is dried in vacuo at about 50° C. to give 81 g of 5-carboxyphthalide with a titer (HPLC)>94% and purity (HPLC)>95%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703516B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-9d706995746b4fbd82ba867be377cf54
Quellennotizuspto-grants-2004_03