HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-(4,5,6,7-Tetrahydrobenzothiazol-2-ylmethoxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoate | HCID 19611521 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4,5,6,7-Tetrahydrobenzothiazol-2-ylmethoxy)benzoic acid | HCID 19611578 | 75% |
Reaction Steps
A mixture of methyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoate (361 mg, 1.2 mmol), tetrahydrofuran (2 ml), methanol (2 ml) and 1 N sodium hydroxide (2 ml) was stirred at room temperature for 12 hours and then concentrated under reduced pressure. The resulting residue was dissolved in water and the solution was adjusted to pH 3 by adding 10% citric acid aqueous solution. Thereafter, the solid substance formed was collected by filtration, washed with water, and then dried under reduced pressure to give 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoic acid (257 mg, 0.89 mmol, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981559 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-a7e677c24d794a738ca9e02d5e8b4ac4 |
| Source note | uspto-grants-1999_11 |