Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | HCID 20467498 | HCID 20467498 | — |
| Reactant | HCID 178511117 | HCID 178511117 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Anthraquinone | HCID 6780 | 254.4% |
Reaction Steps
To a solution of 1-amino-2-(2-hydroxyphenyloxy)-4-hydroxy-5-chloroanthraquinone (3.82 g) in tetrahydrofuran (50 ml), N,N-diethylaniline (1.7 g) and 2,4-difluoro-6-(β-cyanoethyl)aminotriazine (1.85 g) were added and the mixture was subjected to condensation as in Example 3. The reaction liquor was treated as in Example 1 to produce 5.3 g of anthraquinone dye (λ max in acetone=527 nm) of the following formula in a yield of 93%. ##STR12## A dye dispersion was made from a mixture of the anthraquinone dye (16 parts), polyoxyethylene glycol nonylphenyl ether with an HLB of 13.3 (7 parts), naphthalene-sulfonic acid-formaldehyde condensate (3 parts) and water (74 parts) by grinding it with a sand grinder. Using the dye dispersion, a padding bath having the following formulation was prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436906 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-0c03064c424546caa497e8f838000a1c |
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| Source note | uspto-grants-1984_03 |
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