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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 973364생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/973364

반응식

참여 물질

역할이름HCID투입량
반응물DiazaldHCID 6628—
반응물DiazomethaneHCID 9550—
반응물Potassium HydroxideHCID 14797—
반응물o-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acidHCID 15029348—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물Methyl o-(1-hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoateHCID 1502935226%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05062881
출처 데이터셋uspto-grants-1991_11
ORD IDord-ccccce07ac934270a6cb5b1eb987a777
출처 메모uspto-grants-1991_11