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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508303Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochlorideHCID 73902—
Reactant2,3-dimethyl-5-sulfo-1,3-di(4-sulfobutyl)-3H-indoliumHCID 58490238—
SolventAcOH AcOAcHCID 21895370—
Product4-[2-[6-anilino-1,3,5-hexatrienyl]-3-methyl-5-sulfo-3-(4-sulfobutyl)-3H-1-indoliumyl]-1-butanesulfonateHCID 8669534366.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095612B2
Source datasetuspto-grants-2015_08
ORD IDord-cb08a2ebd89547888a95bf1a38c5ffb1
Source noteuspto-grants-2015_08