Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochloride | HCID 73902 | — |
| 반응물 | 2,3-dimethyl-5-sulfo-1,3-di(4-sulfobutyl)-3H-indolium | HCID 58490238 | — |
| 용매 | AcOH AcOAc | HCID 21895370 | — |
| 생성물 | 4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonate | HCID 86695343 | 66.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09095612B2 |
| 출처 데이터셋 | uspto-grants-2015_08 |
| ORD ID | ord-cb08a2ebd89547888a95bf1a38c5ffb1 |
| 출처 메모 | uspto-grants-2015_08 |