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HRID 1707560作成日:2026年10月26日

Diazald → Methyl o-(1-hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoate

https://huagongshe.com/reaction/1707560

反応式

関与物質

役割名称HCID仕込み量
反応物DiazaldHCID 6628—
反応物DiazomethaneHCID 9550—
反応物Potassium HydroxideHCID 14797—
反応物o-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acidHCID 15029348—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl o-(1-hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoateHCID 1502935226%

反応手順

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-D-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05354727
出典データセットuspto-grants-1994_10
ORD IDord-e1443e7c651043b6b3df041894eaaf60
出典メモuspto-grants-1994_10