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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595069Generated: October 30, 2026

Sodium ethoxide → Diethyl acetamide 2-(4-octanoyl phenyl)ethyl malonate

https://huagongshe.com/reaction/1595069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant4-(2-Bromoethyl)octanophenoneHCID 21707523—
ReactantDiethyl acetamide malonateHCID 22466969—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductDiethyl acetamide 2-(4-octanoyl phenyl)ethyl malonateHCID 86757349—

Reaction Conditions

Temperature60 °C

Reaction Steps

The fraction which contains 4-(2-bromoethyl)octanophenone prepared in the step N (500 mg) was dissolved in anhydrous ethanol (2 ml) to obtain a solution. Sodium ethylate (164 mg) was added to the solution. The mixture was stirred under atmosphere of nitrogen at 60° C. for 1 hour. The suspension was dissolved in N,N-dimethylformamide (10 ml) to obtain a solution. Diethyl acetamide malonate (1050 mg) and sodium ethylate (245 mg) were added to the solution, and the solution was stirred under atmosphere of nitrogen at 60° C. overnight. The reaction solution was poured into ice water, extracted with ether, and washed with saturated saline solution. The extracted solution was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography using hexane-ethyl acetate (1:0e3:1) as an eluate to obtain diethyl acetamide-2-(4-octanoyl phenyl)ethyl malonate (477 mg) in the form of colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284915B1
Source datasetuspto-grants-2001_09
ORD IDord-355534a247e14e3b8226fd574da83dd5
Source noteuspto-grants-2001_09