HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676354Generated: November 2, 2026
HCID 67350060, compound → HCID 67348734, compound
https://huagongshe.com/reaction/1676354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67350060 | HCID 67350060 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Catalyst | Manganese triacetate dihydrate | HCID 12416832 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67348734 | HCID 67348734 | 12.1% |
Reaction Steps
A solution of methyl 3-(allyl(4-fluorophenyl)amino)-3-oxopropanoate (10 g, 39.7 mmol) in acetic acid (50 mL) was added into a suspension of manganese (III) acetate dihydrate (21 g, 79.7 mmol) and copper (II) acetate monohydrate (7.9 g, 39.7 mmol) in acetic acid (200 mL). The reaction was allowed to stir for 3 days at room temperature. The reaction was quenched with 10% aqueous sodium bisulfite solution (100 mL). The reaction mixture was diluted with EtOAc, washed with saturated aqueous NaHCO3, brine, dried with Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography (50% EtOAc in hexane) to afford the product (1.2 g, 12% yield) as a brown power. LRMS (APCI pos) m/e 250.1 (M+1). 1H NMR: (CDCl3, 400 MHz) δ 7.49-7.54 (m, 2H), 7.02-7.07 (m, 2H), 4.02-4.07 (m, 1H), 3.83 (s, 3H), 3.70 (d, 1H), 2.45-2.53 (m, 1H), 2.02-2.09 (m, 1H), 1.29-1.33 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003662B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-4b1f6b9350544b578b4b14b063c3b45b |
|---|
| Source note | uspto-grants-2011_08 |
|---|