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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676354Generated: November 2, 2026

HCID 67350060, compound → HCID 67348734, compound

https://huagongshe.com/reaction/1676354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67350060HCID 67350060—
CatalystCupric acetate monohydrateHCID 165397—
CatalystManganese triacetate dihydrateHCID 12416832—
SolventAcetic AcidHCID 176—
ProductHCID 67348734HCID 6734873412.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-4b1f6b9350544b578b4b14b063c3b45b
Source noteuspto-grants-2011_08