HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 1,2,3,4-tetrahydro-6-methoxy-1-oxo-2-naphthaleneacetate → HCID 13934508, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 1,2,3,4-tetrahydro-6-methoxy-1-oxo-2-naphthaleneacetate | HCID 13934507 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 13934508 | HCID 13934508 | — |
Reaction Steps
A solution of the 6-methoxy-1-tetralone derivative (860 mg) (from Example 13) in 47% HBr (15 ml) and glacial acetic acid (5 ml) was refluxed for 30 hours and poured into ice-water. The product was extracted into ethyl acetate (3×) and the combined organic extracts were washed with brine, dried over Na2SO4 and concentrated to dryness. The residue was esterified with 10% HCl in methanol to give, after work-up, the title compound, m.p. 121°-123°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983628 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-55a17fa363f24074ac76f249fe3f2335 |
| Source note | uspto-grants-1991_01 |