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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2166856생성일: 2026년 10월 27일

p-Toluenesulfonic acid → Butanoic acid, 3-[[5-(acetylamino)-2-methoxyphenyl]amino]-, ethyl ester

https://huagongshe.com/reaction/2166856

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Ethyl AcetoacetateHCID 8868—
반응물4'-Methoxy-3'-nitroacetanilideHCID 95043—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
용매IsopropanolHCID 3776—
생성물Butanoic acid, 3-[[5-(acetylamino)-2-methoxyphenyl]amino]-, ethyl esterHCID 17281898%

반응 단계

A mixture of 105.0 g. (0.5 mole) of 2-nitro-4-acetamidoanisole, 67.0 g. (0.5 mole) of ethyl acetoacetate, 550 ml. of isopropyl alcohol, 10.0 g. of 5% Pt/C, and 3.0 g. of p-toluenesulfonic acid is treated in an autoclave at 165° C. and 1,000 psi of hydrogen until the uptake of hydrogen ceases. The solvent and catalysts are removed. Upon standing, 143.8 g. (98%) of ethyl 3-(2'-methoxy-5-acetamidoanilino)butyrate is obtained. NMR analysis of the product supports the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04389531
출처 데이터셋uspto-grants-1983_06
ORD IDord-451eded8c84b4688af791421495fb604
출처 메모uspto-grants-1983_06