Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20501123 | HCID 20501123 | — |
| Reactant | HCID 73681569 | HCID 73681569 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86738893 | HCID 86738893 | — |
Reaction Steps
A solution of 3 ml of triethylamine in 100 ml of dimethylsulfoxide was added to 4 g of 1-(2-carboxyethyl)-4-(4-anilino-1,3-butadien-1-yl)-quinolinium bromide and 3 g of 3-(2-methylnaphtho[1,2-d]thiazolin-1-yl)-propane-1-sulfonate and the resulting mixture was subjected to reaction at 100° C. for 2 hours. After completion of the reaction, the reaction product was cooled, and diethyl ether was added, after which the resulting precipitate was collected by filtration to obtain a crude dye. It was boiled together with ethanol to obtain crystals, and the crystals were recrystallized from methanol containing a small quantity of triethylamine to obtain 0.9 g of the objective compound (melting point 219° C.) which was dark green. Its maximum absorption wavelength as measured in triethylamine-containing methanol was 760 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04386146 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-02c9f105cb6342478dd485eac7d40e2f |
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| Source note | uspto-grants-1983_05 |
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