HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroethane → 2-Naphthol-6-sulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroethane | HCID 6337 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-Acetyl-(1-amino-2-naphthol-6-sulfonic acid) | HCID 133359 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Naphthol-6-sulfonic acid | HCID 7117 | — |
| Product | N-Acetyl-(1-amino-2-naphthol-6-sulfonic acid) | HCID 133359 | — |
| Product | 2-Naphthalenesulfonic acid, 5-amino-6-ethoxy- | HCID 222166 | — |
Reaction Steps
12.5 parts of 1-acetamino-2-hydroxy-naphthalene-6-sulphonic acid (67.5% pure=8.5 parts of 100% pure), prepared according to Example 4, and 4.2 parts of potassium carbonate are suspended in a mixture of 47.4 parts by weight of methanol and 9.0 parts by weight of water in an autoclave. After heating the autoclave, 6.2 parts of 25% strength potassium hydroxide solution and 5.8 parts of ethyl chloride are simultaneously metered in at 120° C. The reaction mixture is worked up analogously to Example 12. 87% of theory of 1-amino-2-ethoxy-naphthalene-6-sulphonic acid, relative to 1-acetamino-2-hydroxy-naphthalene-6-sulphonic acid, or 67.8% of theory, relative to 2-hydroxy-naphthalene-6-sulphonic acid, are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04341719 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-d9d6743fe5a84dddb35021e780b3007d |
| Source note | uspto-grants-1982_07 |