HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-METHOXYISOBENZOFURAN-1(3H)-ONE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | o-Hydroxyphthalsaure | HCID 22292283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-METHOXYISOBENZOFURAN-1(3H)-ONE | HCID 11116379 | — |
| Product | o-Methoxyphthalsaure | HCID 19598034 | — |
Reaction Steps
Anhydrous 2-methoxyphthalic acid (640 mg), which was prepared with using anhydrous 2-hydroxyphthalic acid by the same procedure as reference example 12, was suspended in tetrahydrofuran (20 ml). Acetic acid (430 mg) and sodium borohydride (135 mg) were added to the suspension. The mixture was stirred for 30 min. at room temperature and for 2 hr. at 50° C. The reaction solution was cooled. 1N hydrochloric acid (7 ml) was added to the cooled solution. The solution was stirred for 15 min. The reaction solution was evaporated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1→1:1) to give the title compound (314 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05457122 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-1920310458944ed6910bb40d0ed2e10a |
| Source note | uspto-grants-1995_10 |