Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | 2,6-Naphthalenedicarboxylic acid | HCID 14357 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 22987106 | HCID 22987106 | — |
Reaction Steps
2,6-Dicarboxynaphthalene having carboxyl groups bonded to a naphthalene nucleus, designated compound A, is chosen as a starting compound. Two moles of thionyl chloride is added to one mole of compound A, and the mixture is heated to about 75 to 90° C., preferably about 80° C., with stirring in a nitrogen atmosphere. Then the stirring force is diminished, and the reaction mixture is refluxed for about 6 to 18 hours, desirably about 10 to 12 hours. The bath temperature is set at about 90 to 100° C., at which unreacted thionyl chloride is removed by evaporation over about 2 hours to obtain 2,6-dicarboxychloronaphthalene, designated compound B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06632916B2 |
|---|
| Source dataset | uspto-grants-2003_10 |
|---|
| ORD ID | ord-474bfa7fc8df42e2ad02989461ee8218 |
|---|
| Source note | uspto-grants-2003_10 |
|---|