HuagongsheHuagongshe Chemistry Print Report · For research reference only
21224-20-4 → Methyl 5-(1,3-benzothiazol-2-yl)pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 21224-20-4 | HCID 1971493 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | Methyl 5-(1,3-benzothiazol-2-yl)pentanoate | HCID 18002644 | 67% |
Reaction Steps
A solution of 5-(2-benzothiazolyl)pentanoic acid (1.54 g, 6.5 mmol, prepared according to the procedure of Example 12 in JP, A, 8-208631 (1996)) in hydrochloric acid-methanol (40 ml) was stirred at room temperature overnight, and evaporated. The residue was dissolved in chloroform, and washed with saturated aqueous sodium hydrogen carbonate. The organic layer was dried over anhydrous magnesium sulfate, evaporated, and purified through flash column chromatography to give methyl 5-(2-benzothiazolyl)pentanoate (1.08 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642250B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-6ea897a685174315ac633287610bf07e |
| Source note | uspto-grants-2003_11 |