HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (R)-4-hydroxy-2-(3-methoxybenzyl)cyclopent-2-enone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetate | HCID 71170032 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-4-hydroxy-2-(3-methoxybenzyl)cyclopent-2-enone | HCID 71170057 | 85% |
Reaction Steps
(R)-3-(3-Methoxybenzyl)-4-oxocyclopent-2-enyl acetate (0.1 g, 0.38 mmol) was dissolved in THF (1 ml), 3N HCl (5 ml) was added to the solution, and the mixture was stirred at room temperature overnight. The reaction was quenched with saturated NaHCO3 to pH=6.9 and extracted with EtOAc and the organic layer was washed with brine, dried over MgSO4, and evaporated. The resulting residue was purified by chromatography on a silica gel column using hexane-EtOAc as eluent to give the (R)-4-hydroxy-2-(3-methoxybenzyl)cyclopent-2-enone as yellow oil: 71 mg (yield: 85%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08350090B1 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-649434777df14c7d9a134450507ad1fc |
| Source note | uspto-grants-2013_01 |