Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805521Generated: October 29, 2026

Methyl 4-methoxyacetoacetate → HCID 178496272, compound

https://huagongshe.com/reaction/1805521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-methoxyacetoacetateHCID 123500—
ReactantSodium AcetateHCID 517045—
Reactant2,2,6-Trifluoro-2H-1,3-benzodioxol-5-amineHCID 14405700—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178496272HCID 17849627270%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2,2,6-trifluoro-1,3-benzodioxol-5-amine (4.95 g, 25.9 mmol) in 6 M HCl aqueous solution (25.9 mL) was added a solution of NaNO2 (2.15 g, 31.1 mmol) in water (5.2 mL) at 0° C. To a suspension of methyl 4-methoxy-3-oxobutanoate (3.35 mL, 25.9 mmol) and NaOAc (38.9 g) in EtOH (44 mL) was added the above solution at 0° C. The mixture was stirred at 0° C. for 10 min. The precipitates were collected by filtration, washed with water, dissolved in EtOAc, washed with brine and NaHCO3 aqueous solution, dried over MgSO4, filtered and concentrated in vacuo to yield the title compound (6.31 g, 70% yield) as a red solid: 1H NMR (DMSO-d6, 300 MHz): δ ppm 3.33 (3H, s), 3.82 (3H, s), 4.66 (2H, s), 7.57-7.92 (2H, m), 12.32 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354411B2
Source datasetuspto-grants-2013_01
ORD IDord-a7939cbd894741308d869039bc858756
Source noteuspto-grants-2013_01