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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249192Erstellt: 23. Oktober 2026

Diazald → HCID 15029352, Verbindung

https://huagongshe.com/de/reaction/249192

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiazaldHCID 6628—
EduktDiazomethaneHCID 9550—
EduktPotassium HydroxideHCID 14797—
Edukto-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acidHCID 15029348—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 15029352HCID 1502935226%

Reaktionsschritte

A solution of potassium hydroxide (0.19 g, 0.00339 mol) and ethanol is added portionwise to a 0° C. mixture of Diazald® N-methyl-N-nitroso-p-toluenesulfonamide (0.73 g, 0.0034 mol) and ether. The mixture is kept in an ice-bath for 10 minutes then in an water bath for 10 minutes. The diazomethane is distilled into a mixture of o-(1-hydroxy-4-isopropyl-4-methyl-5-oxo-2-imi-dazolin-2-yl)benzoic acid (0.67 g, 0.00243 mol) and ethanol. After 45 minutes the reaction mixture is quenched with acetic acid and concentrated in vacuo to give an oil. The oil is dissolved into ethyl acetate, dried over anhydrous magnesium sulfate and concentrated in vacuo to yield an off-white solid. The solid is chromatographed using silica gel and methylene chloride/ethyl acetate 3:1 as eluent to give the title compound as a white solid (0.18 g, 26%), mp 146°-150° C., identified by IR and NMR spectral analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05213607
Quelldatensatzuspto-grants-1993_05
ORD IDord-89dfff02494f47cea89400c7958839d0
Quellennotizuspto-grants-1993_05