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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 508303생성일: 2026년 10월 25일

N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochloride → 4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonate

https://huagongshe.com/reaction/508303

반응식

참여 물질

역할이름HCID투입량
반응물N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochlorideHCID 73902—
반응물2,3-dimethyl-5-sulfo-1,3-di(4-sulfobutyl)-3H-indoliumHCID 58490238—
용매AcOH AcOAcHCID 21895370—
생성물4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonateHCID 8669534366.8%

반응 단계

300 mg (0.55 mmol) of 2,3-dimethyl-5-sulfo-1,3-di(4-sulfobutyl)-3H-indolium and 190 mg (0.66 mmol) of N-[5-(phenylamino)-2,4-pentadienylidene]aniline monohydrochloride were heated in 6 mL acetic anhydride-acetic acid (1:1, v/v) mixture for 30 min at 110° C. After cooling the product was precipitated with ethyl acetate, filtered off and washed with ether to give 240 mg (56%) of 4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonate. λmax (abs) 505 nm (methanol). This product was used for following step without additional purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09095612B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-cb08a2ebd89547888a95bf1a38c5ffb1
출처 메모uspto-grants-2015_08