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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 973363Erstellt: 24. Oktober 2026

Sulfuric Acid → o-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acid

https://huagongshe.com/de/reaction/973363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
EduktMethyl 2,3-dimethyl-2-[(1-oxo-2,3-benzoxazin-4-yl)amino]butyrateHCID 15029344—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkto-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acidHCID 1502934876%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

Sodium hydroxide (0.58 g, 0.0145 mol) in water is added to a solution of methyl 2,3-dimethyl-2-[(1-oxo-2,3-benzoxazin-4-yl)amino]butyrate (2.0 g, 0.00689 mol) and tetrahydrofuran under a nitrogen atmosphere. The reaction mixture is stirred at 45° C. for 36 hours then at room temperature for 6 days. The reaction mixture is concentrated in vacuo to give an oil. The oil is dissolved into water. The aqueous solution is cooled with an ice-bath and concentrated sulfuric acid is added until a pH of about 1 is obtained then the solution is extracted with ethyl acetate. The combined ethyl acetate extracts are dried with anhydrous magnesium sulfate and concentrated in vacuo to give a pale yellow solid. The solid is added to boiling methylene chloride and after 2/3 of the methylene chloride has evaporated, the mixture is filtered to give the title compound as a white solid (1.44 g, 76%), mp 186°-188° C., identified by IR and NMR spectral analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05062881
Quelldatensatzuspto-grants-1991_11
ORD IDord-1259cd6509904d89a8ff6231b3c2ba25
Quellennotizuspto-grants-1991_11