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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1069485생성일: 2026년 10월 23일

Acetone → {[2-(7-Methoxy-benzo[1,3]dioxole-5-carbonyl)-benzenesulfonyl]-o-tolyl-amino}-acetic acid methyl ester

https://huagongshe.com/ko/reaction/1069485

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물IsopropanolHCID 3776—
반응물({2-[Hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl esterHCID 22965597—
반응물Jones' reagentHCID 131709961—
용매Ethyl AcetateHCID 8857—
생성물{[2-(7-Methoxy-benzo[1,3]dioxole-5-carbonyl)-benzenesulfonyl]-o-tolyl-amino}-acetic acid methyl esterHCID 2296559659%

반응 단계

To acetone (225 mL) was added ({2-[hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl ester (4.17 g, 8.35 mmol), and 8N Jones reagent (4 mL). The mixture was stirred 15 minutes giving a suspended solid. Isopropanol (20 mL) was added followed by stirring for 15 minutes. The mixture was filtered, saturated sodium bicarbonate solution was added, and the solvent was removed in vacuo giving a paste. The paste was resuspended in ethyl acetate and water, filtered, and washed with saturated sodium bicarbonate, brine and dried over anhydrous magnesium sulfate. The solution was filtered and evaporated to a solid which was crystallized from ethyl acetate and ethyl ether giving a white solid, 2.41 g, 59% yield, mp 159-170° C. NMR spectra and elemental analysis were consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06252070B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-8359ecf4f77845398f2050a98f4449de
출처 메모uspto-grants-2001_06