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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6192생성일: 2026년 10월 24일

3-Mercaptopropionic Acid → N-(4-Anilinophenyl)-3-sulfanylpropanamide

https://huagongshe.com/ko/reaction/6192

반응식

참여 물질

역할이름HCID투입량
반응물3-Mercaptopropionic AcidHCID 6514—
반응물O-XyleneHCID 7237—
반응물N-Phenyl-p-phenylenediamineHCID 7564—
용매HexaneHCID 8058—
생성물N-(4-Anilinophenyl)-3-sulfanylpropanamideHCID 19795022—

반응 조건

온도140 °C

반응 단계

A mixture of 18.4 grams of N-phenyl-p-phenylene diamine, 10.6 grams of β-mercaptopropionic acid and 120 milliliters of xylene (technical grade) was heated to reflux (about 140° C.) under nitrogen atmosphere, with stirring. A 1.6 milliliter quantity of water (90% of theory) was removed from this mixture by azetropic distillation through a Vigreux column with the aid of Dean-Start trap, during a 13-hour period. A solid product was isolated in 18.7 grams quantity from the reaction mixture by cooling the latter, pouring into hexane, collecting the resultant crystalline product by filtration, washing the crushed crystalline product with more hexane and evaporating to dryness. The product was recrystallized from hot toluene to 17.6 grams (64.5%) of white platelets melting at 98.3°-99.5° C. The resultant new compound, N-(4-anilino-phenyl)beta-mercaptopropionamide, sometimes referred to hereafter as MPDA, had mercaptan assay of 93.8% of theoretical, on the basis of a potentiometric titration with an isopropyl alcohol solution of silver nitrate, following a method described R. M. Pierson, A. J. Costanza and A. H. Weinstein, J. Polymer Sci., 17, 234 (1955).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247027
출처 데이터셋uspto-grants-1993_09
ORD IDord-b17abff2b44840dd9b7ca02149e953e2
출처 메모uspto-grants-1993_09