HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-oxo-3-phenylindene-2-carboxylate → Ethyl(1RS)-1-Hydroxy-1-(3,4-methylenedioxyphenyl)-3-phenylindene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-oxo-3-phenylindene-2-carboxylate | HCID 18427658 | — |
| Reactant | HCID 178419615 | HCID 178419615 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl(1RS)-1-Hydroxy-1-(3,4-methylenedioxyphenyl)-3-phenylindene-2-carboxylate | HCID 18969644 | 72% |
Reaction Steps
To a solution of ethyl 1-oxo-3-phenylindene-2-carboxylate (1.0 g, 3.6 mmol) in THF (35 ml) under an argon atmosphere at 0° C. was added a solution of freshly prepared 3,4-methylenedioxyphenyl magnesium bromide (5.4 mmol). After stirring for 30 min, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3 and saturated aqueous NaCl and dried (MgSO4). The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 10% EtOAc/hexanes to afford the title compound (1.03 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719182 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-3fded2dafaa549269661bae8fd2c3503 |
| Source note | uspto-grants-1998_02 |