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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17896생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 1-oxo-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/17896

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl esterHCID 11845282—
용매MethanolHCID 887—
생성물1-oxo-3-phenyl-6-(3-phenyl-propoxy)-1H-indene-2-carboxylic acid methyl esterHCID 6870103575.3%

반응 단계

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate ethyl ester (1.65 g, 4.0 mmol) prepared in (Step 5) of Example 1 was dissolved in methanol (160 ml) and p-toluene sulfonic acid (228 mg, 1.2 mmol) was added thereto. The mixture was reacted for 1 hour at 70° C., and then washed with brine. The organic layer was extracted with ethyl acetate, dried over anhydrous sulfonate sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9) to obtain the title compound (yield 75.3%) as a red solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741323B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3b200dad4b06471d9b74686d147c1eb5
출처 메모uspto-grants-2010_06