HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (2,4-Dimethoxy-1,3-benzothiazol-7-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13814267 | HCID 13814267 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Product | (2,4-Dimethoxy-1,3-benzothiazol-7-yl)acetic acid | HCID 19082155 | — |
Reaction Steps
A solution of (2,4-dimethoxy-1,3-benzothiazol-7-yl)-acetonitrile (3.61 g, J. Med. Chem., 1987, 30, 1166) and potassium hydroxide (3.45 g) in methanol:water (2:1, 150 ml) was heated to reflux for 6.5 hours. The reaction was cooled and the solvents evaporated under reduced pressure. Water (50 ml) was added and the aqueous layer extracted with diethyl ether. The aqueous layer was then acidified to pH4/5 with acetic acid and extracted with ethyl acetate. The combined organic layers were washed (water and brine), dried (MgSO4) and the solvent evaporated under reduced pressure to yield the subtitled compound which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05648370 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-ab424ef3a124419caa8959192e1ac949 |
| Source note | uspto-grants-1997_07 |