HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-[Benzo-1,2,3-thiadiazol-7-yl]acrylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzo[d][1,2,3]thiadiazole-7-carbaldehyde | HCID 14835681 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-[Benzo-1,2,3-thiadiazol-7-yl]acrylic acid | HCID 54496090 | 447.6% |
Reaction Steps
A mixture of 1.96 g of benzo-1,2,3-thiadiazole-7-carbaldehyde, 1.24 g of malonic acid and 6 ml of pyridine are heated for 26 hours at 120° C., with 2 further additions of 0.6 g portions of malonic acid after 4 and 7 hours. The mixture is then cooled, poured into ice-water and acidified with concentrated hydrochloric acid. The precipitate which has formed is faltered off and dissolved in dilute sodium hydroxide solution, the mixture is washed three times with methylene chloride, and the aqueous phase is subsequently acidified once more, using hydrochloric acid. The precipitate obtained is filtered off, washed with water and dried in vacuo, resulting in 11 g of the title compound of m.p. 199°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05384321 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-4ee0d24133594dcb8030147d7c8e9ff5 |
| Source note | uspto-grants-1995_01 |