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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | t-Butyl ethyl 2-allylmalonate | HCID 19809570 | — |
| Reactant | 2-Ethylbenzoyl chloride | HCID 22323683 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | t-Butyl ethyl 2-allyl-2-(2-ethylbenzoyl)malonate | HCID 19809551 | 67.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166377 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-e4feaa6bf8a248a397199913645ea246 |
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| Source note | uspto-grants-1992_11 |
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