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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120120Generated: November 2, 2026

Acetamidomalonic acid diethyl ester → HCID 10547728, compound

https://huagongshe.com/reaction/2120120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantSodium ethoxideHCID 2723922—
Reactant2-(3-Chloropropionyl)-4-methylphenolHCID 10703138—
SolventEthanolHCID 702—
ProductHCID 10547728HCID 1054772889%

Reaction Steps

Diethyl acetamidomalonate (12.84 g, 59.11 mmol) was added to freshly prepared 0.29 M NaOEt (225 ml) in EtOH at 0° C. The solution resulting after brief sonication was transferred to an addition funnel and added over six minutes to a suspension of 20 (10.68 g, 53.74 mmol) in EtOH (50 ml) at 0° C. After stirring the reaction mixture for 18 hours at room temperature, solvent was removed in vacuo. Cold 0.25 N HCl (200 ml) was added and the aqueous phase was extracted with CHCl3 (200 ml, 2×100 ml). The organic layer was washed with H2O (100 ml). After solvent removal, the solid was purified by silica gel flash column chromatography using 4% acetone/—CH2Cl2 to furnish 18.1 g (89%) of diethyl (acetylamino)[3-(2—hydroxy-5-methylphenyl)-3-oxopropyl]propanedioate (I) as a solid: NMR δ 1.26 (t, 6H, J=7), 2.04 (s, 3H), 2.30 (s, 3H), 2.78 (t, 2H, J=7), 2.98 (t, 2H, J=7), 4.17-4.34 (m, 4H), 6.79 (s, 1H), 6.88 (d, 1H, J=8), 7.25-7.30 (m, 1H), 7.47 (s, 1H), 11.97 (s, 1H). Anal. calcd. for C19H25NO7: C 60.15, H 6.64, N 3.69. Found: C 60.23, H 6.73, N 3.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689788B1
Source datasetuspto-grants-2004_02
ORD IDord-c7888b1a499e48928970ae289634ea87
Source noteuspto-grants-2004_02