HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86725322, compound → HCID 86725324, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86725322 | HCID 86725322 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86725324 | HCID 86725324 | 84.5% |
Reaction Steps
Into a glass vial containing the product from step (b) (130 mg, 0.385 mmol) in diethyl ether (5 ml), 2-methoxyphenyl magnesium bromide (3.85 ml, 1.92 mmol) was added. The reaction mixture was stirred at reflux for 30 minutes. The reaction was cooled to room temperature, quenched with of 10% aqueous NH4Cl (50 ml), and extracted with EtOAc (3×). The combined EtOAc extracts were washed with brine, dried over Na2SO4, and the solvent evaporated in vacuo to give the crude product. Purification by silica-gel chromatography (gradient elution: 0 to 40% EtOAc in hexanes) gave the sub-title compound as a yellow oil (145 mg). MS: ESI (positive): 446 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284277B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e1a61930a3214f2e93f19a7400f8cf4e |
| Source note | uspto-grants-2016_03 |