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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374250Generated: October 25, 2026

Sodium hydride → t-Butyl ethyl 2-allyl-2-(2-ethylbenzoyl)malonate

https://huagongshe.com/reaction/374250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantt-Butyl ethyl 2-allylmalonateHCID 19809570—
Reactant2-Ethylbenzoyl chlorideHCID 22323683—
SolventDimethylformamideHCID 6228—
Productt-Butyl ethyl 2-allyl-2-(2-ethylbenzoyl)malonateHCID 1980955167.6%

Reaction Steps

Sodium hydride (2.8 g., 50% w/w dispersion in mineral oil) was added over 15 minutes to an ice cooled solution of t-butyl ethyl 2-allylmalonate (13.4 g.) in dry DMF (120 ml.) under nitrogen. The mixture was stirred at room temperature for 45 minutes and cooled to 0° C. 2-Ethylbenzoyl chloride (10.1 g.) was added over 2 minutes and the mixture stirred at room temperature for 18 hours. The DMF was evaporated and the residue shaken with water (100 ml.) and ethyl acetate (200 ml.). The ethyl acetate phase was separated, washed with saturated brine, dried (MgSO4) and evaporated. The oil obtained (21.8 g.) was purified by flash column chromatography on silica (650 g.) using toluene as eluant to give t-butyl ethyl 2-allyl-2-(2-ethylbenzoyl)malonate (14.3 g.) as an oil; NMR: 1.25 (15H,m), 2.7 (2H,q), 2.9 (2H,d), 4.12 (2H,q), 5.31 (2H,m), 6.05 (1H,m) and 7.35 (4H,m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166377
Source datasetuspto-grants-1992_11
ORD IDord-e4feaa6bf8a248a397199913645ea246
Source noteuspto-grants-1992_11