Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Chloroethane | HCID 6337 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Amino-2-naphthol-6-sulfonic acid | HCID 145804 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20530992 | HCID 20530992 | — |
Reaction Steps
According to Examples 2 and 3 of German Democratic Republic Pat. No. 9,728, 1-amino-2-ethoxy-naphthalene-6-sulphonic acid, is obtained by a procedure in which, in a first stage, 1-acetamino-2-hydroxy-naphthalene-6-sulphonic acid is prepared from 1-amino-2-hydroxy-naphthalene-6-sulphonic acid by reaction with acetic anhydride in dilute acetic acid, this intermediate product is etherified, in a second stage, with diethyl sulphate or with ethyl chloride in aqueous-alcoholic sodium hydroxide solution to give 1-acetamino-2-ethoxy-naphthalene-6-sulphonic acid, and, finally, this intermediate product is deacetylated, without intermediate isolation, by heating with aqueous sodium hydroxide solution to give 1-amino-2-ethoxy-naphthalene-6-sulphonic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04341719 |
|---|
| Source dataset | uspto-grants-1982_07 |
|---|
| ORD ID | ord-387f3205b27849f8b30fe898c781f3aa |
|---|
| Source note | uspto-grants-1982_07 |
|---|