HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Aminoterephthalic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl aminoterephthalate | HCID 79336 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Aminoterephthalic acid | HCID 2724822 | 89% |
Reaction Steps
A representative preparation was done as follows: Dimethyl aminoterephthalate (5 g), cetyltrimethyl ammonium bromide catalyst (0.05 g) and aqueous NaOH solution (5%, 300 ml) were taken in a 500 ml round bottom flask, and heated to and held at about 60° C. for about 2 hours. The mixture was then cooled to about 15°-20° C., and acidified with concentrated HCl when the acid of Formula 3 separated as yellow crystals. This was filtered, washed with ice cold water, and dried (yield: 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264539 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-a8157de3536c4b3ab4ef96abe13fc8c2 |
| Source note | uspto-grants-1993_11 |