Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Reactant | 4-Aminophenethyl alcohol | HCID 66904 | — |
| Reactant | 1,8-Dinitro-4,5-dihydroxyanthraquinone | HCID 3378440 | — |
| Reactant | 2-(4-Aminophenyl)propane-1,3-diol | HCID 19593976 | — |
| Product | 2-Phenylethanol | HCID 6054 | — |
Reaction Steps
A mixture of 19.4 g of 1,8-dihydroxy-4,5-dinitroanthraquinone, 25.0 g of a mixture consisting of about 72 % of 2-(4-aminophenyl)-ethanol, about 22 % of 2-(4-aminophenyl)propane-1,3-diol, about 3 % of 4-toluidine and by-products, and 140 g of diethylene glycol monomethyl ether is heated to 130° C. over a period of 2.5 hours. Stirring at 130-135° C. is continued for 6 hours, during which the water of the reaction is separated off by distillation. The reaction mixture is cooled to 100° C. and stirred into a mixture of 250 g of water, 250 g of ice and 110 g of 32 % hydrochloric acid. This crude dye suspension is filtered at about 20° C., and the product is washed with about 3 liters of water. After drying, 27 g of a dye mixture containing 65 % of the dye of the formula ##STR12## 13 % of the dye of the formula ##STR13## 3 % of the dye of the formula ##STR14## 7% of 1,8-dihydroxy-4-nitro-5-aminoanthraquinone, and 2-phenylpropane-1,3-diol and phenylethanol is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04964876 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-8ba5088737a041269298dfc4a45f7de2 |
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| Source note | uspto-grants-1990_10 |
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