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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703364Generated: October 29, 2026

Diethyl Malonate → HCID 22149831, compound

https://huagongshe.com/reaction/703364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantHCID 54562802HCID 54562802—
SolventEthanolHCID 702—
SolventSodiumHCID 5360545—
ProductHCID 22149831HCID 22149831—

Reaction Steps

In a 1.0 liter flask was dissolved 2.4 g (0.104 mol) of freshly cut sodium metal in 10 mL of absolute ethanol. To this solution was added a solution of 15.6 g (0.0975 mol) of diethyl malonate in 25 mL of absolute ethanol followed by a solution of 30.2 g (0.0928 mol) of 1-(4-(5-(trifluoromethyl)-3-fluoro-2-pyridyloxy)phenyl)but-1-en-3-one in 75 mL of absolute ethanol. The mixture was stirred at ambient temperature for 6 hours and a cream colored solid precipitated from the solution. The mixture was then diluted with 250 mL of water and the solid slowly dissolved therein. To this solution was slowly added 12 mL of concentrated HCl and the desired product crystallized out of the solution. The product was recovered by filtration, thoroughly washed with water and dried in vacuo. The product melted at 161°-163° C., with decomposition; Rf -0.32 (silica gel, 10:90 MeOH:CHCl3), 1H NMR (CDCl3): δ 1.0 (t, 3H, CH3CH2 --), 2.3-3.1 (m, 2H, ring protons), 3.4-3.75 (m, 2H, ring protons), 3.96 (q, 2H, CH3CH2 --), 5.39 (s, 1H, vinyl), 7.10-8.2 (m, 6H, aromatic), 9.0-11.7 (b, 1H, --OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983211
Source datasetuspto-grants-1991_01
ORD IDord-c5a8da1d780c42e09c42254e8b86d8e2
Source noteuspto-grants-1991_01