HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochloride | HCID 73902 | — |
| Edukt | 2,3-dimethyl-5-sulfo-1,3-di(4-sulfobutyl)-3H-indolium | HCID 58490238 | — |
| Lösungsmittel | AcOH AcOAc | HCID 21895370 | — |
| Produkt | 4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonate | HCID 86695343 | 66,8% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09095612B2 |
| Quelldatensatz | uspto-grants-2015_08 |
| ORD ID | ord-cb08a2ebd89547888a95bf1a38c5ffb1 |
| Quellennotiz | uspto-grants-2015_08 |