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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667356Generated: October 31, 2026

Ethyl 2-methylacetoacetate → HCID 57937746, compound

https://huagongshe.com/reaction/1667356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromopentyl acetateHCID 85140—
SolventTolueneHCID 1140—
ProductHCID 57937746HCID 5793774649%

Reaction Steps

In a 1 L three necked flask equipped with a mechanical stirrer and reflux condenser was placed dry toluene (300 ml). The system was flushed with argon and sodium hydride (Aldrich, 60% dispersion in mineral oil) (7.2 g, 1.2 eq.) was added. Ethyl-α-methylacetoacetate (Aldrich, 21 g, 0.15 mole) was added with stirring over a 30 minutes. The resulting solution was heated under reflux for 2 hours and cooled slightly. (Note: Reaction mixture becomes a thick paste and a mechanical stirrer is essential). 5-Bromopentylacetate (Aldrich, 31.5 g, 15 mol) was added (all at once) and the suspension was heated under reflux for 12 hr, cooled, filtered and the solvent evaporated under reduced pressure. The residue was distilled under vacuum to yield 20 g (45%) of colorless liquid, b.p 90-92 (0.5 mm). 1H NMR in CDCl3 δ, 4.1-4.2 (m, 2H, O—CH2CH3): 3.5 (t, J=7 Hz, 2H, CH2OCO—); 2.2 (s, 3H, CH3CO); 2.1 (s, 3H, —COCH3); 1.5-2.0 (m, 10H, 4-(CH2)2, C—CH3, OCH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044203B2
Source datasetuspto-grants-2011_10
ORD IDord-490654611b544660b33cd141531e8b61
Source noteuspto-grants-2011_10